NDC 0591-3332

NDC 0591-3332

NDC 0591-3332 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0591-3332
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0591-3332-30 [00591333230]

Bupropion Hydrochloride XL TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077715
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-06-13
Marketing End Date2015-07-31

NDC 0591-3332-05 [00591333205]

Bupropion Hydrochloride XL TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077715
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-03-11
Marketing End Date2015-07-31

NDC 0591-3332-19 [00591333219]

Bupropion Hydrochloride XL TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077715
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-08-28
Marketing End Date2015-07-31

NDC 0591-3332-10 [00591333210]

Bupropion Hydrochloride XL TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077715
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-06-13
Marketing End Date2015-07-31

Drug Details

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.