NDC 63629-6659

NDC 63629-6659

NDC 63629-6659 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 63629-6659
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 63629-6659-2 [63629665902]

PredniSONE TABLET
Marketing CategoryANDA
Application NumberANDA087342
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-10
Marketing End Date2018-08-31

NDC 63629-6659-5 [63629665905]

PredniSONE TABLET
Marketing CategoryANDA
Application NumberANDA087342
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-10
Marketing End Date2018-08-31

NDC 63629-6659-6 [63629665906]

PredniSONE TABLET
Marketing CategoryANDA
Application NumberANDA087342
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-10
Marketing End Date2018-08-31

NDC 63629-6659-1 [63629665901]

PredniSONE TABLET
Marketing CategoryANDA
Application NumberANDA087342
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-10
Marketing End Date2018-08-31

NDC 63629-6659-3 [63629665903]

PredniSONE TABLET
Marketing CategoryANDA
Application NumberANDA087342
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-10
Marketing End Date2018-08-31

NDC 63629-6659-4 [63629665904]

PredniSONE TABLET
Marketing CategoryANDA
Application NumberANDA087342
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-10
Marketing End Date2018-08-31

Drug Details

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