"57237-033-75" National Drug Code (NDC)

NDC Code	57237-033-75
Package Description	75 mL in 1 BOTTLE (57237-033-75)
Product NDC	57237-033
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amoxicillin
Non-Proprietary Name	Amoxicillin
Dosage Form	POWDER, FOR SUSPENSION
Usage	ORAL
Start Marketing Date	20061228
Marketing Category Name	ANDA
Application Number	ANDA065334
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	AMOXICILLIN
Strength	400
Strength Unit	mg/5mL
Pharmacy Classes	Penicillin-class Antibacterial [EPC], Penicillins [CS]