NDC 58118-3268

NDC 58118-3268

NDC 58118-3268 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 58118-3268
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 58118-3268-9 [58118326809]

Venlafaxine Hydrochloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA022104
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-04-29
Marketing End Date2017-06-21

NDC 58118-3268-8 [58118326808]

Venlafaxine Hydrochloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA022104
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-04-29
Marketing End Date2017-06-21

NDC 58118-3268-0 [58118326800]

Venlafaxine Hydrochloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA022104
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-04-29
Marketing End Date2017-06-21

NDC 58118-3268-3 [58118326803]

Venlafaxine Hydrochloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA022104
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-04-29
Marketing End Date2017-06-21

Drug Details

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