NDC 54868-4033

NDC 54868-4033

NDC 54868-4033 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 54868-4033
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 54868-4033-2 [54868403302]

Morphine Sulfate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075295
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-06-30
Inactivation Date2019-09-24

NDC 54868-4033-0 [54868403300]

Morphine Sulfate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075295
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-06-30
Inactivation Date2019-09-24

NDC 54868-4033-3 [54868403303]

Morphine Sulfate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075295
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-06-30
Inactivation Date2019-09-24

NDC 54868-4033-1 [54868403301]

Morphine Sulfate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075295
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-06-30
Inactivation Date2019-09-24

NDC 54868-4033-5 [54868403305]

Morphine Sulfate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075295
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-06-30
Inactivation Date2019-09-24

NDC 54868-4033-4 [54868403304]

Morphine Sulfate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075295
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-06-30
Inactivation Date2019-09-24

Drug Details

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.