NDC 54868-3732

NDC 54868-3732

NDC 54868-3732 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 54868-3732
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 54868-3732-0 [54868373200]

MEBENDAZOLE TABLET, CHEWABLE
Marketing CategoryANDA
Application NumberANDA073580
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1996-04-04
Inactivation Date2019-09-24

NDC 54868-3732-2 [54868373202]

MEBENDAZOLE TABLET, CHEWABLE
Marketing CategoryANDA
Application NumberANDA073580
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1996-04-04
Inactivation Date2019-09-24

NDC 54868-3732-3 [54868373203]

MEBENDAZOLE TABLET, CHEWABLE
Marketing CategoryANDA
Application NumberANDA073580
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1996-04-04
Inactivation Date2019-09-24

Drug Details


© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.