NDC 16590-835

NDC 16590-835

NDC 16590-835 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 16590-835
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 16590-835-45 [16590083545]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA078206
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-07-30
Inactivation Date2019-10-29

NDC 16590-835-90 [16590083590]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA078206
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-07-30
Inactivation Date2019-10-29

NDC 16590-835-56 [16590083556]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA078206
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-07-30
Inactivation Date2019-10-29

NDC 16590-835-60 [16590083560]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA078206
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-07-30
Inactivation Date2019-10-29

NDC 16590-835-72 [16590083572]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA078206
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-07-30
Inactivation Date2019-10-29

NDC 16590-835-50 [16590083550]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA078206
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-07-30
Inactivation Date2019-10-29

NDC 16590-835-30 [16590083530]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA078206
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-07-30
Inactivation Date2019-10-29

NDC 16590-835-75 [16590083575]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA078206
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-07-30
Inactivation Date2019-10-29

Drug Details

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