NDC 16590-373

NDC 16590-373

NDC 16590-373 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 16590-373
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 16590-373-90 [16590037390]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA080292
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-05-22
Inactivation Date2019-11-27

NDC 16590-373-60 [16590037360]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA080292
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-05-22
Inactivation Date2019-11-27

NDC 16590-373-48 [16590037348]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA080292
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-05-22
Inactivation Date2019-11-27

NDC 16590-373-30 [16590037330]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA080292
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1972-05-22
Inactivation Date2019-11-27

NDC 16590-373-21 [16590037321]

PREDNISONE TABLET
Marketing CategoryANDA
Application NumberANDA080292
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1972-05-22
Inactivation Date2019-11-27

Drug Details

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.