"57237-333-01" National Drug Code (NDC)

NDC Code	57237-333-01
Package Description	100 TABLET in 1 BOTTLE (57237-333-01)
Product NDC	57237-333
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Meclizine Hcl
Non-Proprietary Name	Meclizine Hydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20240722
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M009.10
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	MECLIZINE HYDROCHLORIDE
Strength	12.5
Strength Unit	mg/1
Pharmacy Classes	Antiemetic [EPC], Emesis Suppression [PE]