"57237-098-01" National Drug Code (NDC)

NDC Code	57237-098-01
Package Description	100 mL in 1 BOTTLE (57237-098-01)
Product NDC	57237-098
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Cefadroxil
Non-Proprietary Name	Cefadroxil
Dosage Form	POWDER, FOR SUSPENSION
Usage	ORAL
Start Marketing Date	20130425
Marketing Category Name	ANDA
Application Number	ANDA065349
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	CEFADROXIL
Strength	500
Strength Unit	mg/5mL
Pharmacy Classes	Cephalosporin Antibacterial [EPC], Cephalosporins [CS]