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Last Updated: December 22, 2024

Details for New Drug Application (NDA): 206975


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NDA 206975 describes BUPROPION HYDROCHLORIDE, which is a drug marketed by Accord Hlthcare, Actavis Labs Fl Inc, Anbison Lab, Annora Pharma, Aurobindo Pharma Usa, Endo Operations, Epic Pharma Llc, Granules, Graviti Pharms, Impax Labs, Invagen Pharms, Jubilant Generics, Lupin Ltd, Prinston Inc, Rising, Sandoz, Sciegen Pharms Inc, Sinotherapeutics Inc, Sun Pharm, Torrent, Twi Pharms, Watson Labs Inc, Wockhardt Ltd, Yichang Humanwell, Zhejiang Jutai Pharm, Zydus Pharms, Alembic, Apnar Pharma Lp, Apotex Inc, Cadila Pharms Ltd, Heritage Pharma, Invatech, and Micro Labs, and is included in fifty-nine NDAs. It is available from seventy-two suppliers. Additional details are available on the BUPROPION HYDROCHLORIDE profile page.

The generic ingredient in BUPROPION HYDROCHLORIDE is bupropion hydrochloride. There are thirty-eight drug master file entries for this compound. Seventy-seven suppliers are listed for this compound. Additional details are available on the bupropion hydrochloride profile page.
Summary for 206975
Tradename:BUPROPION HYDROCHLORIDE
Applicant:Heritage Pharma
Ingredient:bupropion hydrochloride
Patents:0
Suppliers and Packaging for NDA: 206975
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
BUPROPION HYDROCHLORIDE bupropion hydrochloride TABLET;ORAL 206975 ANDA NCS HealthCare of KY, LLC dba Vangard Labs 0615-8261 0615-8261-39 30 TABLET in 1 BLISTER PACK (0615-8261-39)
BUPROPION HYDROCHLORIDE bupropion hydrochloride TABLET;ORAL 206975 ANDA NCS HealthCare of KY, LLC dba Vangard Labs 0615-8296 0615-8296-39 30 TABLET in 1 BLISTER PACK (0615-8296-39)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength75MG
Approval Date:Aug 19, 2016TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength100MG
Approval Date:Aug 19, 2016TE:ABRLD:No

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