NDC 54868-4921

NDC 54868-4921

NDC 54868-4921 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 54868-4921
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 54868-4921-3 [54868492103]

Labetalol Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074787
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-12-31
Inactivation Date2019-09-24

NDC 54868-4921-1 [54868492101]

Labetalol Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074787
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-05-06
Inactivation Date2019-09-24

NDC 54868-4921-0 [54868492100]

Labetalol Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074787
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-05-06
Inactivation Date2019-09-24

NDC 54868-4921-4 [54868492104]

Labetalol Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074787
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-04-04
Inactivation Date2019-09-24

NDC 54868-4921-2 [54868492102]

Labetalol Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074787
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-05-06
Inactivation Date2019-09-24

Drug Details

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