Smoking Cessation
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Sign up freeTop drugs studied for this disease
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FDA approval · 2010-07-08FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Apnar Pharma LP)
FDA approved a supplemental application for bupropion hydrochloride from Apnar Pharma LP, approving changes associated with this generic pro…
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FDA approval · 2010-07-08FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (BluePoint Laboratories)
FDA approves BluePoint Laboratories' supplemental application for Bupropion Hydrochloride under ANDA 076143, approving changes to the approv…
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FDA approval · 2010-06-29FDA Approved: NICOTROL — Supplemental Application (Pharmacia & Upjohn Company LLC)
FDA approved a supplemental application for NICOTROL (nicotine) submitted by Pharmacia & Upjohn Company LLC.
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FDA approval · 2010-06-17FDA Approved: EQUATE NICOTINE — Supplemental Application (Wal-Mart Stores Inc)
The FDA approved a supplemental application for Equate Nicotine (nicotine polacrilex gum) from Wal-Mart Stores Inc under ANDA078326.
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FDA approval · 2010-06-17FDA Approved: QUITINE NICOTINE — Supplemental Application (QUITINE LLC)
The FDA approved a supplemental application for QUITINE NICOTINE (nicotine polacrilex) from QUITINE LLC.
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FDA approval · 2010-05-13FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
The FDA approved a supplemental application for Bupropion hydrochloride from Amneal Pharmaceuticals of New York LLC, authorizing a generic v…
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FDA approval · 2010-04-21FDA Approved: NICORETTE 4MG FRUIT CHILL GUM, LIL DRUG STORE — Supplemental Application (Lil' Drug Store Products, Inc.)
FDA approved a supplemental application for NICORETTE 4MG FRUIT CHILL GUM manufactured by Lil' Drug Store Products, Inc., adding this produc…
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FDA approval · 2010-04-21FDA Approved: NICORETTE ORIGINAL — Supplemental Application (Haleon US Holdings LLC)
FDA approved a supplemental application for NICORETTE ORIGINAL (nicotine polacrilex) from Haleon US Holdings LLC.
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FDA approval · 2010-03-25FDA Approved: EQUATE NICOTINE — Supplemental Application (Wal-Mart Stores Inc)
FDA approved a supplemental application for EQUATE NICOTINE (nicotine polacrilex), a nicotine replacement therapy gum. The product is manufa…
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CLINICAL_TRIALS trial_result · 2010-03-11Clinical Trial Update: Nicotine Patch Trial in Syrian Primary Care Settings [Phase 2]
A Phase 2 clinical trial evaluating a nicotine patch for smoking cessation in Syrian primary care settings has completed.
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FDA approval · 2010-02-04FDA Approved: CHANTIX — Supplemental Application (Pfizer Laboratories Div Pfizer Inc)
FDA approved a supplemental application for Chantix (varenicline tartrate) from Pfizer Laboratories Div Pfizer Inc, updating the CHANTIX lab…
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FDA approval · 2010-01-27FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
FDA approved a supplemental application for bupropion hydrochloride (generic) submitted by Amneal Pharmaceuticals of New York LLC under ANDA…
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CLINICAL_TRIALS trial_result · 2010-01-11Clinical Trial Update: An Investigation Of The Effects Of Food On The Absorption Of A Varenicline Controlled Release Formulation [Phase 1]
Phase 1 study evaluating the effect of food on the absorption of a varenicline controlled-release formulation. The trial has completed.
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FDA approval · 2010-01-05FDA Approved: NICORETTE — Supplemental Application (Haleon US Holdings LLC)
FDA approved a supplemental application for Nicorette (nicotine polacrilex) submitted by Haleon US Holdings LLC.
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FDA approval · 2009-11-16FDA Approved: BUPROPION HYDROCHLORIDE SR — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for Bupropion Hydrochloride SR from Actavis, a generic sustained-release formulation.
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FDA approval · 2009-11-05FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Epic Pharma LLC)
FDA approved a supplemental application for bupropion hydrochloride (Epic Pharma LLC) under ANDA 075932. This approval updates the approved …
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FDA approval · 2009-07-10FDA Approved: NICOTINE — Original Application (Walgreen Company)
FDA approved Walgreens' original application for nicotine polacrilex gum (nicotine replacement therapy) to aid adults in quitting smoking an…
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FDA approval · 2009-07-10FDA Approved: KIRKLAND SIGNATURE NICOTINE — Original Application (Costco Wholesale Company)
FDA approves Costco Wholesale Company's Kirkland Signature Nicotine (nicotine polacrilex) under an Original Application, making it available…
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FDA approval · 2009-07-08FDA Approved: NICOTINE — Original Application (P & L Development, LLC)
FDA approved NICOTINE POLACRILEX (nicotine polacrilex lozenges) from P & L Development, LLC under an original application (ANDA079044).
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FDA approval · 2009-05-18FDA Approved: NICORETTE — Original Application (Haleon US Holdings LLC)
FDA approved NICORETTE (nicotine polacrilex) under Original Application NDA022360 by Haleon US Holdings LLC for smoking cessation. NICORETTE…
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FDA approval · 2009-05-06FDA Approved: NICORETTE ORIGINAL — Supplemental Application (Haleon US Holdings LLC)
FDA approved a supplemental application for NICORETTE ORIGINAL (nicotine polacrilex) from Haleon US Holdings LLC.
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FDA approval · 2009-05-06FDA Approved: NICORETTE 4MG FRUIT CHILL GUM, LIL DRUG STORE — Supplemental Application (Lil' Drug Store Products, Inc.)
FDA approved a supplemental application for Nicorette 4 mg Fruit Chill Gum from Lil' Drug Store Products, Inc. (nicotine polacrilex).
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CLINICAL_TRIALS trial_result · 2009-03-13Clinical Trial Update: Nicotine Substitute Prescribed at Hourly Intake or ad Libitum for Heavy Smokers Willing to Quit [Phase 4]
A Phase 4 trial conducted by the University of Lausanne evaluated nicotine replacement therapy administered hourly or ad libitum for heavy s…
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FDA approval · 2009-03-02FDA Approved: RUGBY NICOTINE POLACRILEX GUM, ORIGINAL FLAVOR — Supplemental Application (Rugby Laboratories)
FDA approves a supplemental application for Rugby Nicotine Polacrilex Gum, Original Flavor, a generic nicotine replacement gum (ANDA).
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FDA approval · 2008-12-19FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Apnar Pharma LP)
The FDA approved a supplemental application for bupropion hydrochloride submitted by Apnar Pharma LP.