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post #61 of 86
6/10/12 at 7:10pm

BULLISH WEDGE CONFIRMED ABOUT TO BREAK OUTTTTTTTTTTTTTTTTTTTTTTTTTTTT booyah.gif

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post #62 of 86
6/11/12 at 7:14am
Thread Starter 

IPCI IS THE BEST AND THE MOST UNDERVALUED UNKNOWN GEM IN THE BIOTECH SECTOR BUT PLEASE DO YOUR OWN RESEARCH ! GLTA

This Unknown ULTRA LOW FLOAT Stock awaiting 6 FDA approvals which will be all approved within 10 months.IPCI has 15 Drugs in Pipeline many nearing ANDA/NDA filing including a potential Blockbuster .

Market Cap 45 Mil / Cash 7.5 M / Burn-rate 4.5 M per Year = Enough Cash until Profitability which will happen THIS YEAR .

3-4 FDA APPROVALS IN 2012 = $10++ EASILY FOLKS ! GLTA

This sleeping giant will be another billion dollar company in the near term .

Intellipharmaceutics (IPCI)

Market Cap:$ 45 M
Cash: $ 7.5 M
Price: $2.83

Shares Out: 15.9 Mil..(10 Mil Shares held by Insiders/Institutions)

SUPER LOW FLOAT: 4 M


Intellipharmaceutics now has six ANDAs being reviewed by the FDA for approval, with reported sales by others for branded and generic versions of these products being approximately $6.6 billion for the 12 months ended September 2011. The Company develops both ANDA product candidates and new drugs through the New Drug Application (NDA) 505(b)(2) regulatory pathway.



MONSTER Pipeline
http://www.intellipharmaceutics.com/pipeline.cfm


Latest Presentation :
http://www.intellipharmaceutics.com/common/download/download.cfm?companyid=ABEA-43EQSZ&fileid=559152&filekey=daac778d-c51b-47b3-9ad8-7917dcd3ce57&filename=Intellipharmaceutics%20Presentation%20April%202012%20Website.pdf


New Article (IPCI worth $15++ per share )
http://seekingalpha.com/article/308884-intellipharmaceutics-a-deep-value-opportunity-in-generics-and-specialty-pharmaceuticals?source=yahoo


CEO says multiple deals, FDA approvals and more filings are in the works
http://www.biomedreports.com/2011042166212/ceo-says-multiple-deals-fda-approvals-and-filings-are-in-the-works.html

..........................

Roth starts Intellipharmaceutics at buy

Roth Capital Partners has initiated coverage of Intellipharmaceutics (NASDAQ:IPCI; TSX:I) with a “buy” rating , saying the emerging generics company could launch four new products in the coming 12-to-18 months.

“We believe that this momentum could unlock value for this under covered stock,” writes analyst Scott Henry. The stock closed at $2.97 on Wednesday.

Intellipharmaceutics’ four upcoming product launches include generics of Focalin XR, Effexor XR, Protonix, and Glucophage XR. The lead product, Focalin XR for attention deficit hyperactivity disorder, is partnered with generic leader Par Pharmaceuticals.

“This product pipeline produces branded revenue near $5 billion and we believe that these generic offerings could produce near $100 million in end-user revenue potential for Intellipharmaceutics,” Mr. Henry points out.

He figures product launches could boost revenue from about $1 million in 2011 to nearly $20 million in 2013, with the company crossing over into profitability in the fourth quarter of 2012. For 2013, he predicts earnings per share of 30 cents.

Intellipharmaceutics also has an “entrant in the high-growth area of abuse-resistant opioids, which could be a multi-billion dollar market,” Mr. Henry said. “Although early, this gives investors another way to win, in our opinion.”

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post #63 of 86
6/12/12 at 2:36pm

Yes it is continuing to go up plus 2% today!

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post #64 of 86
6/12/12 at 10:01pm

Another Blockbuster On Deck for Intellipharmaceutics? 
By M.E. Garza 

http://top10stocks-china.blogspot.ca/2012/06/another-blockbuster-on-deck-for.html 

We were surprised to see that shares of Intellipharmaceutics (IPCI) barely reacted after the company announced that it has retained the services of Doll Consulting's David S. Doll, to assist with the commercialization of products in its controlled-release generic drug portfolio as well as its New Drug Application (NDA) portfolio. 

If the news was not fully digested as a positive development, then its a safe bet that investors also missed the “Easter egg” in Monday's press release. Fellow nerds may know that a virtual Easter egg is an intentional hidden message, in-joke or feature in movies, books or video games. The term draws a parallel with the custom of the Easter egg hunt observed which thrives on discovering hidden surprises. We’ll come back to the Easter egg momentarily. 

As we’ve saying, IPCI is an intriguing biotech play with an extremely low float. The stock ran to $6 after we issued a detailed report describing why we expect it to become a multi-bagger. Every time it dips, we’ve been encouraging our readers to diligently accumulate more shares. They’d be smart to do so in light of Monday’s news. 

First, it tells us that the firm is finally about to enter the commercialization phase. It also suggests that FDA approvals are on the way and as we've said recently, that positions IPCI well for partnership offers for the distribution of their super generic drug formulations. Intellipharmaceutics’ master drug formulator and CEO, Isa Odidi and his team have been busy filing controlled released versions with the FDA. 

The news also tells us that Odidi is willing to do what it takes to make sure investors in the company get back the best value they can. By enlisting Doll, Odidi brings on an expert in commercial pharmaceutical operations with an impressive resume spanning over 26 years in the pharmaceutical industry. Doll’s stint as executive vice president, commercial operations at Impax Laboratories (IPXL) shows that he can successfully negotiate lucrative, long-term agreements with the major pharmaceutical companies who want IPCI’s products. Doll has already done it on multiple occasions with TEVA (TEVA), Shire Plc. (SHP), Novartis (NVS), Purdue Pharma, Schering (BYERF.PK), Wyeth (WYE), and others. 

Here’s a direct quote from Monday’s press release. See if you can spot the Easter egg: 

"We now have four products filed with the FDA for the purpose of obtaining regulatory approval in the U.S. [ANDA's for Focalin XR, Effexor XR, Protonix, Glucophage XR] and expect to file at a minimum an additional two products this year," stated Dr. Isa Odidi, CEO and co-Founder of Intellipharmaceutics. "Given our progress last year, our anticipated growth moving forward, and an increased focus on partnering due to our advancing pipeline, Dave Doll, with his impressive track record in business development and commercialization, is an excellent addition to our team." 

Did you see it? If you spotted the reference in Odidi’s quote to “Glucophage XR,” then you’re on to something. 

This is the first time we have ever seen Glucophage XR mentioned in any public disclosure as a drug that Intellipharmaceutics has submitted to the FDA. Did we miss the press release disclosing this previously or has that news yet to make the wires? 

People had been betting that Odidi would be going after yet another big market drug, but I don’t think anyone had guessed that it would be the first-line drug of choice for the treatment of type 2 diabetes- Glucophage. Bristol Myers Squibb (BMY) and others have made billions marketing the drug. Diabetes affects roughly 6% of the adult population; somewhere north of 246 million people worldwide, and the number is expected to rise to 380 million by 2025. With doctors and experts at the International Diabetes Federation recommending that drug remains a drug of choice for first-line therapy of type 2 diabetes, there is clearly plenty of room in the market for the version IPCI has submitted for approval. 

Odidi has also told the market that IPCI will be filing at least two more products this year. That gives us more reason to be excited. Smart money says those will be multi-billion dollar drugs as well. 

As we pointed out in our initial report, Investors are excited about a potential NDA filing with the FDA for Abuse Resistant Oxycontin. Controlled-release oxycodone drugs had U.S. sales of approximately $2 billion and IPCI's drug delivery platform (branded Rexista) is a novel, paste-in-a-capsule dosage form designed to be a deterrent to the well-documented abuses. Last summer, the company advised investors that it had taken delivery of and fully qualified its primary manufacturing equipment for the manufacture of the abuse-deterrent formulation and that the manufacture of clinical batches using that equipment had commenced. It is worth noting that the company's Rexista technology is applicable to additional opioid drug candidates like oxymorphone, hydrocodone, and morphine. 

The Intellipharmaceutics story is getting more interesting every day. 

Disclosure: Long IPCI

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post #65 of 86
6/17/12 at 4:56pm

TSI & MACD turning around it's getting really juicy here people!!!

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post #66 of 86
6/19/12 at 3:24pm

More then the avg volume today looking nice!

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post #67 of 86
6/20/12 at 7:36pm

Look at all this juicy volume that came in today along with this after hours buying!!! GET READY FOR THE POP HERE PEOPLE!!!

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post #68 of 86
6/21/12 at 9:39pm

OVER $1 MILLION IN ACCUMULATION TODAY AND HUGE VOLUME CAME IN!!! THE FDA APPROVAL IS COMING PEOPLE GET READY!!! booyah.gifkoolaid.gif

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post #69 of 86
6/30/12 at 11:51pm

http://seekingalpha.com/article/673491-the-bio-pharma-momentum-movers-list-for-thursday-june-21?source=yahoo

 

 

IntelliPharmaCeutics International Inc. (IPCI): Yesterday's closing price: $3.05, up Up 0.25 (8.93%) on roughly 3 times its average volume.

ICPI engages in the research, development, and manufacture of novel or generic controlled and targeted release oral solid dosage drugs. The company's patented Hypermatrix technology is a multidimensional controlled-release drug delivery platform that can be applied to the development of various existing and new pharmaceuticals. It has a pipeline of products in various stages of development in therapeutic areas, including neurology, cardiovascular, and gastrointestinal tract, pain, and infection.

Intellipharmaceutics' previously announced development goals for 2012 included the completion of a pre-Investigational New Drug ("pre-IND") meeting with the Food and Drug Administration ("FDA") to discuss its Rexista™ oxycodone development plan. The meeting with FDA officials clarified the company's path going forward for its Rexista™ abuse-deterrent oxycodone development plan.

Intellipharmaceutics is planning to advance toward the next goals of its Rexista program, namely the manufacture of clinical batches of Rexista abuse-deterrent oxycodone product candidate under current good manufacturing practice ("cGMP") conditions and the commencement of definitive Phase I clinical studies.

This follows from the previous proof-of-concept Phase I clinical study completed on a pilot laboratory batch, which yielded positive results.

IPCI might be seeing the beginning of a run-up here in anticipation of news forthcoming on the commencement/progress of the Phase 1 clinical studies of Rexista. The price action I saw yesterday on IPCI is similar to the price action I saw with MDGN before Wednesday's massive pop.

Shares Outstanding: 15.93M
Float: 7.99M
% Held by Insiders: 39.16%
% Held by Institutions: 0.60%
Shares Short (as of May 31, 2012): 125.01K
Short Ratio (as of May 31, 2012): 10.10

As we can see above, with 15.93M shares outstanding, IPCI's market cap comes out to $48.60M - yet another undervalued market cap. With 7.99M shares available to trade, IPCI is definitely a low floating stock.

It is my opinion the volume will increase here at least in the short term, to potentially move the price per share upwards over $3.50 in short order. $4.25 is within reach on a possible catalyst news release.

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post #70 of 86
7/13/12 at 4:09am

VERY SOLID PRESENTATION GIVEN AND HERE IS THE LINK FOR THE PDF SUPER JUICY PEOPLE...GET IN NOW!!!

 

http://www.keepandshare.com/doc/4288041/intellipharmaceutics-presentation-retailinvestor-conference-july-12-2012-pdf-july-13-2012-1-0?da=y

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post #71 of 86
7/13/12 at 1:18pm

Here is another link to view the Presentation since the megabytes got EXCEEDED!!!

 

https://docs.google.com/open?id=0B-osPZqizqd7YVJCdl9WWlBXWDg

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post #72 of 86
8/6/12 at 2:27pm

Looking good for a breakout koolaid.gif

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post #73 of 86
8/14/12 at 1:22pm

Confirmed double bottom!!! Looking for a UPRISE TILL FDA APPROVAL NOW!!!

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post #74 of 86
9/5/12 at 3:43pm

http://www.4-traders.com/news/Intellipharmaceutics-International-Inc-Intellipharmaceutics-Achieves-a-2012-Goal-by-Filing-Two-AN--14490241/

 

 

 

Intellipharmaceutics International Inc. : Intellipharmaceutics Achieves a 2012 Goal by Filing Two ANDAs -- Generic Forms of Keppra XR(R) and Pristiq(R)

09/05/2012 | 09:56am US/Eastern


Seventh and Eighth ANDAs Filed

TORONTO, Sept. 5, 2012 (GLOBE NEWSWIRE) -- Intellipharmaceutics International Inc. (Nasdaq:IPCI) (TSX:I), a pharmaceutical company specializing in the research, development and manufacture of novel and generic controlled-release and targeted-release oral solid dosage drugs, today announced the achievement of another of its previously announced development goals for 2012 with its filing of two Abbreviated New Drug Applications ("ANDAs") with U.S. Food and Drug Administration ("FDA"). The first ANDA is for a generic version of the marketed drug Keppra XR® (levetiracetam extended-release tablets), an antiepileptic drug indicated for the treatment of partial onset seizures in patients with epilepsy. The second ANDA is for a generic version of the marketed drug Pristiq® (desvenlafaxine extended-release tablets), a selective serotonin and norepinephrine reuptake inhibitor indicated for the treatment of major depressive disorder. According to Wolters Kluwer Health, U.S. sales for the 12 months ending July 2012 for Keppra XR® were approximately $149 million and for Pristiq® were approximately $626 million.

"We are pleased to achieve our goal for 2012 of two additional ANDA filings for the year," commented Dr. Isa Odidi, CEO of Intellipharmaceutics. "Our Hypermatrix technology platform is versatile, providing opportunities to replicate release profiles of many drugs with different physical and chemical properties. We continue to expand our controlled-release generic product pipeline, which we believe may provide multiple opportunities for potential revenue generation."

Intellipharmaceutics has now announced eight ANDAs as having been filed with the FDA, with reported sales by others for branded and generic versions of these products being approximately $4.5 billion for the 12 months ended July 2012. The Company develops both ANDA product candidates and new drugs through the New Drug Application (NDA) 505(b)(2) regulatory pathway. There can be no assurance as to whether or when the FDA will approve any Intellipharmaceutics' application.

 

About Intellipharmaceutics

Intellipharmaceutics International Inc. is a pharmaceutical company specializing in the research, development and manufacture of novel and generic controlled-release and targeted-release oral solid dosage drugs. The Company's patented Hypermatrix™ technology is a multidimensional controlled-release drug delivery platform that can be applied to the efficient development of a wide range of existing and new pharmaceuticals. Based on this technology, Intellipharmaceutics has a pipeline of product candidates in various stages of development, including eight ANDAs as having been filed with the FDA, in therapeutic areas that include neurology, cardiovascular, gastrointestinal tract, diabetes, pain and infection.

Certain statements in this document constitute "forward-looking statements" within the meaning of the United States Private Securities Litigation Reform Act of 1995 and/or "forward-looking information" under the Securities Act (Ontario). These statements include, without limitation, statements expressed or implied regarding our plans, goals and milestones, status of developments or expenditures relating to our business, plans to fund our current activities, statements concerning our partnering activities, health regulatory submissions, strategy, future operations, future financial position, future sales, revenues and profitability, projected costs, and market penetration. In some cases, you can identify forward-looking statements by terminology such as "may," "will," "should," "expects," "plans," "anticipates," "believes," "estimates," "predicts," "potential," "continue," "intends," "could," or the negative of such terms or other comparable terminology. We made a number of assumptions in the preparation of our forward-looking statements. You should not place undue reliance on our forward-looking statements, which are subject to a multitude of known and unknown risks and uncertainties that could cause actual results, future circumstances or events to differ materially from those stated in or implied by the forward-looking statements. Risks, uncertainties and other factors that could affect our actual results include, but are not limited to, the effects of general economic conditions, securing and maintaining corporate alliances, our estimates regarding our capital requirements, and the effect of capital market conditions and other factors, including the current status of our product development programs, on capital availability, the potential dilutive effects of any future financing, our programs regarding research, development and commercialization of our product candidates, the timing of such programs, the timing, costs and uncertainties regarding obtaining regulatory approvals to market our product candidates, and the timing and amount of any available investment tax credits, the actual or perceived benefits to users of our drug delivery technologies and product candidates as compared to others, our ability to maintain and establish intellectual property rights in our drug delivery technologies and product candidates, the actual size of the potential markets for any of our product candidates compared to our market estimates, our selection and licensing of product candidates, our ability to attract distributors and collaborators with the ability to fund patent litigation and with acceptable development, regulatory and commercialization expertise and the benefits to be derived from such collaborative efforts, sources of revenues and anticipated revenues, including contributions from distributors and collaborators, product sales, license agreements and other collaborative efforts for the development and commercialization of product candidates, our ability to create an effective direct sales and marketing infrastructure for products we elect to market and sell directly, the rate and degree of market acceptance of our products, the timing and amount of insurance reimbursement for our products, the success and pricing of other competing therapies that may become available, our ability to retain and hire qualified employees, and the manufacturing capacity of third-party manufacturers that we may use for our products. Additional risks and uncertainties relating to the Company and our business can be found in the "Risk Factors" section of our latest annual information form and latest Form 20-F, as well as in our reports, public disclosure documents and other filings with the securities commissions and other regulatory bodies in Canada and the U.S. The forward-looking statements are made as of the date hereof, and we disclaim any intention and have no obligation or responsibility, except as required by law, to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

CONTACT: Intellipharmaceutics

         30 Worcester Road

         Toronto, ON Canada M9W 5X2

         www.intellipharmaceutics.com

         

         Shameze Rampertab

         Vice President Finance & CFO

         416-798-3001 x106

         investors@intellipharmaceutics.com
 
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post #75 of 86
9/11/12 at 3:14pm

Brean Murray Carret & Co. initiates coverage on IntelliPharmaCeutics International (NASDAQ: IPCI) with a Buy. PT $7.00.

Brean analyst said, "We see several near-term catalysts for Intellipharmaceutics, notably its second Phase 1 Rexista dataset, a potential Rexista partnership, and initiation of Phase 3 Rexista trials. Positive Phase 1 data for Rexista could lead to a partnership that generates a significant upfront payment. Also, Phase 3 initiation, expected in 1Q13, would clarify Rexista’s potential market timing."

For an analyst ratings summary and ratings history on IntelliPharmaCeutics International click here. For more ratings news on IntelliPharmaCeutics International click here.

Shares of IntelliPharmaCeutics International closed at $2.86 yesterday, with a 52 week range of $2.40-$3.82.

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post #76 of 86
9/21/12 at 5:39pm

IPCI Technical Analysis

 
 
5 Minutes
 
 
10 Minutes
 
 
15 Minutes
 
 
30 Minutes
 
 
Hourly
 
 
5 Hours
 
 
Daily
 
Summary:
STRONG BUY
Moving Averages:
STRONG BUY
 
Indicators:
BUY

Pivot PointsTime: 21.09.12 21:23 GMT
 
Name S3 S2 S1 Pivot Points R1 R2 R3
Classic 2.58 2.67 2.75 2.84 2.92 3.01 3.09
Fibonacci 2.67 2.73 2.78 2.84 2.9 2.95 3.01
Camarilla 2.77 2.79 2.8 2.84 2.84 2.85 2.87
Woodie's 2.56 2.66 2.73 2.83 2.9 3 3.07
DeMark's - - 2.79 2.86 2.96 - -
Moving AveragesTime: 21.09.12 21:23 GMT
 
Name MA5 MA10 MA20 MA50 MA100 MA200
Simple 2.9117
BUY		 2.9018
BUY		 2.9189
BUY		 2.8420
BUY		 2.8999
BUY		 2.9239
BUY
Exponential 2.9042
BUY		 2.9111
BUY		 2.8872
BUY		 2.8761
BUY		 2.8928
BUY		 2.9791
SELL
Technical IndicatorsTime: 21.09.12 21:23 GMT
 
Name Value Action
RSI(14) 53.208 NEUTRAL
STOCH(9,6) 63.343 BUY
STOCHRSI(14) 59.826 BUY
MACD(12,26) 0.015 BUY
ADX(14) 26.896 SELL
Williams %R -31.423 BUY
Name Value Action
CCI(14) -38.0709 NEUTRAL
ATR(14) 0.1121 Less Volatility
Highs/Lows(14) 0.0000 NEUTRAL
Ultimate Oscillator 55.903 BUY
ROC -1.399 SELL
Bull/Bear Power(13) -0.0560 SELL
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post #77 of 86
10/2/12 at 6:30pm
Intellipharmaceutics Announces Third Quarter 2012 Results
 
TORONTO, Oct. 2, 2012 (GLOBE NEWSWIRE) -- Intellipharmaceutics International Inc. (IPCI) (TSX:I), a pharmaceutical company specializing in the research, development and manufacture of novel and generic controlled-release and targeted-release oral solid dosage drugs, today reported the results of operations for the three and nine months ended August 31, 2012. All dollar amounts referenced herein are in United States dollars unless otherwise noted.
 
The Company recorded a net loss for the three months ended August 31, 2012 of $1.5 million, or $0.08 per common share, compared with net income of $1.1 million, or $0.05 per diluted common share for the three months ended August 31, 2011. The net loss for the nine months ended August 31, 2012 was $4.8 million, or $0.28 per common share, compared with a net loss of $3.6 million, or $0.24 per common share for the nine months ended August 31, 2011. The Company's net loss in the three months ended August 31, 2012, when compared to the net income in the three months ended August 31, 2011, can be attributed to the prior period's fair value adjustment of the derivative liability, as described below, and revenue from the amendment of the existing development and commercialization agreement between the Company and Par Pharmaceutical, Inc. to include additional strengths of Focalin XR(R) generic products. The fair value adjustment of the derivative liability for the three months ended August 31, 2012 was $0.5 million versus $2.5 million in the comparable prior period. There was nil revenue in the current period and revenue of $0.5 million was recognized in the prior period from the $0.6 million cash payment received on the amendment of the existing development and commercialization agreement with Par Pharmaceutical, Inc.
 
Loss from operations for the three months ended August 31, 2012 was $2.1 million compared with $1.4 million for the three months ended August 31, 2011. Research and development expense for the three months ended August 31, 2012 increased to $1.3 million compared to $1.2 million in the three months ended August 31, 2011. After adjusting for stock-based compensation expense, expenditures for research and development for the three months ended August 31, 2012 were lower by $0.1 million. Selling, general and administrative expenses for the three months ended August 31, 2012 increased to $0.7 million versus $0.6 million in the prior period. After adjusting for stock-based compensation expense, expenditures for selling, general and administrative expenses for the three months ended August 31, 2012 were higher by $0.1 million in comparison to the prior period.
 
At August 31, 2012, Intellipharmaceutics' cash and cash equivalents totaled $2.9 million, compared with $4.9 million at May 31, 2012. The decrease in cash during the three months ended August 31, 2012 is mainly a result of cash used in operating activities related to research and development activities.
For the three months ended August 31, 2012 net cash flows used in operating activities increased to $1.6 million, as compared to net cash flows used in operating activities for the three months ended August 31, 2011 of $1.3 million. During these periods the Company incurred similar cash expenditures in research and development activities and for selling, general and administrative expenses. The current periods' increase in cash flows used in operating activities can be attributed to the prior periods' cash receipt in the three months ended August 31, 2011 of $0.6 million from Par Pharmaceutical, Inc. based on the terms of the expanded agreement for development and commercialization of Focalin XR(R) generics. In the prior three month period this was partially offset by the foreign exchange loss of $0.1 million compared to the current three month period foreign exchange gain of $0.2 million. For the three months ended August 31, 2012 net cash flows used in investing activities of $0.4 million related mainly to the purchase of production, laboratory and computer equipment due to the acceleration of product development activities.
 
Corporate Update
In July 2012, the Company reached an agreement with AstraZeneca Pharmaceuticals LP and AstraZeneca UK Limited (collectively "AstraZeneca") to settle all outstanding patent litigation concerning its abbreviated new drug application ("ANDA") for the commercialization in the United States of a generic version of the AstraZeneca drug product, Seroquel XR(R) (quetiapine fumarate extended-release) tablets. On July 30, 2012, and pursuant to the settlement, AstraZeneca and the Company filed proposed Consent Judgments in the District Court for the Southern District of New York to conclude the litigation, subject to other regulatory review. The settlement provides, in part, that the Company is permitted to launch its generic versions of the 50, 150, 200, 300 and 400 mg strengths of Seroquel XR(R), on November 1, 2016, or earlier in certain circumstances, subject only to prior U.S. Food and Drug Administration ("FDA") approval of the Company's ANDA for those strengths. All other terms of the settlement are confidential.
 
In September 2012, the Company announced the achievement of another of its previously announced development goals for 2012 with its filing of two ANDAs with the FDA. The first ANDA was for a generic version of the marketed drug Keppra XR(R) (levetiracetam extended-release tablets), an antiepileptic drug indicated for the treatment of partial onset seizures in patients with epilepsy. The second ANDA was for a generic version of the marketed drug Pristiq(R) (desvenlafaxine extended-release tablets), a selective serotonin and norepinephrine reuptake inhibitor indicated for the treatment of major depressive disorder. According to Wolters Kluwer Health, U.S. sales ("TRx MBS Dollars") for the 12 months ending August 2012 for Keppra XR(R) were approximately $146 million and for Pristiq(R) were approximately $627 million.
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post #78 of 86
10/4/12 at 4:41pm

Looks like a breakout is about to HAPPEN!!! 

 

$3.20 AFTER HOURS NOW!!!

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post #79 of 86
10/4/12 at 4:55pm

You may be onto something. Are you paid though? Seems like a lot of pumping. 

 

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post #80 of 86
10/4/12 at 7:33pm

Nope not at all just been invested into this company since 2011 May.

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