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Generated: August 22, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 200695

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NDA 200695 describes BUPROPION HYDROCHLORIDE, which is a drug marketed by Prinston Inc, Teva, Impax Labs, Sandoz, Actavis Labs Fl Inc, Anchen Pharms, Sciegen Pharms Inc, Anbison Lab Co Ltd, Mylan, Wockhardt Ltd, Apotex Inc, Watson Labs Inc, Invagen Pharms, Jubilant Generics, Sun Pharma Global, Zydus Pharms Usa Inc, Torrent Pharms Ltd, Sandoz Inc, Heritage Pharma, and Lupin Ltd, and is included in forty-two NDAs. It is available from sixty-eight suppliers. Additional details are available on the BUPROPION HYDROCHLORIDE profile page.

The generic ingredient in BUPROPION HYDROCHLORIDE is bupropion hydrochloride. There are thirty-seven drug master file entries for this compound. Seventy-three suppliers are listed for this compound. Additional details are available on the bupropion hydrochloride profile page.

Summary for NDA: 200695

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:0
Therapeutic Class:Antidepressants
Antidotes, Deterrents, and Toxicologic Agents
Formulation / Manufacturing:see details

Suppliers and Packaging for NDA: 200695

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
BUPROPION HYDROCHLORIDE
bupropion hydrochloride
TABLET, EXTENDED RELEASE;ORAL 200695 ANDA Sun Pharma Global FZE 47335-954 47335-954-13 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-13)
BUPROPION HYDROCHLORIDE
bupropion hydrochloride
TABLET, EXTENDED RELEASE;ORAL 200695 ANDA Sun Pharma Global FZE 47335-954 47335-954-81 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-81)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength150MG
Approval Date:Dec 18, 2014TE:AB3RLD:No


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Serving 500+ biopharmaceutical companies globally:

McKinsey
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Mallinckrodt
US Army
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Baxter
Johnson and Johnson
Fish and Richardson
US Department of Justice
Citi

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