"57237-101-01" National Drug Code (NDC)

NDC Code	57237-101-01
Package Description	100 TABLET, FILM COATED in 1 BOTTLE (57237-101-01)
Product NDC	57237-101
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Metoprolol Tartrate
Non-Proprietary Name	Metoprolol Tartrate
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20070911
Marketing Category Name	ANDA
Application Number	ANDA077739
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	METOPROLOL TARTRATE
Strength	50
Strength Unit	mg/1
Pharmacy Classes	Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]