Tobacco Use Disorder
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Sign up freeTop drugs studied for this disease
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FDA approval · 2012-04-25FDA Approved: FOSTER AND THRIVE NICOTINE — Supplemental Application (Strategic Sourcing Services LLC)
FDA approved a supplemental application for Foster and Thrive Nicotine (nicotine polacrilex) submitted by Strategic Sourcing Services LLC.
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FDA approval · 2012-02-15FDA 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 · 2012-02-01FDA Approved: NICORETTE 4MG FRUIT CHILL GUM, LIL DRUG STORE — Supplemental Application (Lil' Drug Store Products, Inc.)
The FDA approved a supplemental application to allow Lil' Drug Store Products, Inc. to market Nicorette 4 mg Fruit Chill Gum (nicotine polac…
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FDA approval · 2012-02-01FDA 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 · 2012-01-20FDA Approved: CHANTIX — Supplemental Application (Pfizer Laboratories Div Pfizer Inc)
The FDA approved a supplemental application for CHANTIX (varenicline tartrate) submitted by Pfizer Laboratories Div Pfizer Inc. The approval…
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FDA approval · 2011-12-15FDA Approved: BASIC CARE NICOTINE — Supplemental Application (Amazon.com Services LLC)
FDA approved a supplemental application for BASIC CARE NICOTINE (nicotine polacrilex) from Amazon.com Services LLC, confirming it as an appr…
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FDA approval · 2011-11-09FDA Approved: CHANTIX — Supplemental Application (Pfizer Laboratories Div Pfizer Inc)
The FDA approved a supplemental application for CHANTIX (varenicline tartrate) from Pfizer Laboratories Div Pfizer Inc.
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FDA approval · 2011-10-31FDA Approved: DG HEALTH NICOTINE — Supplemental Application (Dolgencorp Inc)
FDA approves a supplemental application for DG Health Nicotine (nicotine polacrilex) by Dolgencorp Inc, a nicotine replacement therapy indic…
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FDA approval · 2011-09-27FDA Approved: NICORETTE 4MG FRUIT CHILL GUM, LIL DRUG STORE — Supplemental Application (Lil' Drug Store Products, Inc.)
The FDA approved a supplemental application for NICORETTE 4MG FRUIT CHILL GUM from Lil' Drug Store Products, Inc., confirming continued regu…
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FDA approval · 2011-07-22FDA Approved: CHANTIX — Supplemental Application (Pfizer Laboratories Div Pfizer Inc)
The FDA approved a supplemental application for Chantix (varenicline tartrate) from Pfizer Laboratories Div Pfizer Inc., indicating an updat…
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FDA approval · 2011-05-17FDA 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 · 2011-05-17FDA Approved: NICORETTE 4MG FRUIT CHILL GUM, LIL DRUG STORE — Supplemental Application (Lil' Drug Store Products, Inc.)
FDA approved a supplemental application to market NICORETTE 4MG FRUIT CHILL GUM by Lil' Drug Store Products, Inc. (nicotine polacrilex) for …
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FDA approval · 2010-06-25FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for Bupropion Hydrochloride from Actavis Pharma, Inc., bringing this generic product under the appro…
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FDA approval · 2010-06-17FDA Approved: GOOD NEIGHBOR PHARMACY NICOTINE — Supplemental Application (Amerisource Bergen)
FDA approved a supplemental application for GOOD NEIGHBOR PHARMACY NICOTINE (NICOTINE POLACRILEX) submitted by Amerisource Bergen.
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FDA approval · 2010-06-17FDA Approved: NICOTINE — Supplemental Application (H E B)
FDA approved a supplemental application for nicotine polacrilex (nicotine) submitted by H E B, expanding the approved product under an exist…
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FDA approval · 2010-06-17FDA Approved: FOSTER AND THRIVE NICOTINE — Supplemental Application (Strategic Sourcing Services LLC)
FDA lists a supplemental application for Foster and Thrive Nicotine (nicotine polacrilex) from Strategic Sourcing Services LLC, with the sub…
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FDA approval · 2010-04-22FDA Approved: CHANTIX — Supplemental Application (Pfizer Laboratories Div Pfizer Inc)
FDA approved a supplemental application for CHANTIX (varenicline tartrate) submitted by Pfizer Laboratories Div Pfizer Inc.
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FDA approval · 2010-04-05FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Epic Pharma LLC)
The FDA approved a supplemental application for Bupropion hydrochloride from Epic Pharma LLC, granting approval for this generic product.
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FDA approval · 2010-02-16FDA Approved: NICOTINE TRANSDERMAL SYSTEM — Supplemental Application (Aveva Drug Delivery Systems, Inc.)
FDA approved a supplemental application for Aveva Drug Delivery Systems' Nicotine Transdermal System, expanding regulatory clearance for thi…
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FDA approval · 2009-12-21FDA Approved: NICORETTE — Supplemental Application (Haleon US Holdings LLC)
The FDA approved a supplemental application for NICORETTE (nicotine polacrilex) from Haleon US Holdings LLC.
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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 · 2009-07-08FDA Approved: NICOTINE — Original Application (P & L Development, LLC)
FDA approved the original ANDA for nicotine polacrilex, a nicotine replacement therapy product, submitted by P & L Development, LLC.
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FDA approval · 2009-07-08FDA Approved: NICOTINE — Original Application (Lucy Goods, Inc.)
FDA approved the original ANDA for NICOTINE POLACRILEX (nicotine) by Lucy Goods, Inc., enabling a generic nicotine replacement product to en…
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FDA approval · 2009-07-01FDA Approved: CHANTIX — Supplemental Application (Pfizer Laboratories Div Pfizer Inc)
FDA approved a supplemental application for Chantix (varenicline tartrate) from Pfizer, authorizing changes to the product labeling.
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FDA approval · 2009-07-01FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (BluePoint Laboratories)
FDA approves a supplemental application for Bupropion hydrochloride (ANDA 076143) submitted by BluePoint Laboratories.