NDC 54868-5310

NDC 54868-5310

NDC 54868-5310 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 54868-5310
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 54868-5310-6 [54868531006]

Azathioprine TABLET
Marketing CategoryANDA
Application NumberANDA077621
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-09-05
Inactivation Date2019-09-24

NDC 54868-5310-2 [54868531002]

Azathioprine TABLET
Marketing CategoryANDA
Application NumberANDA077621
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-05-23
Marketing End Date2012-06-28

NDC 54868-5310-0 [54868531000]

Azathioprine TABLET
Marketing CategoryANDA
Application NumberANDA077621
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-05-23
Inactivation Date2019-09-24

NDC 54868-5310-5 [54868531005]

Azathioprine TABLET
Marketing CategoryANDA
Application NumberANDA077621
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-06-28
Inactivation Date2019-09-24

NDC 54868-5310-1 [54868531001]

Azathioprine TABLET
Marketing CategoryANDA
Application NumberANDA077621
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-05-23
Marketing End Date2012-06-28

NDC 54868-5310-4 [54868531004]

Azathioprine TABLET
Marketing CategoryANDA
Application NumberANDA077621
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-05-23
Inactivation Date2019-09-24

NDC 54868-5310-3 [54868531003]

Azathioprine TABLET
Marketing CategoryANDA
Application NumberANDA077621
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-05-23
Inactivation Date2019-09-24

Drug Details

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