"67253-148-45" National Drug Code (NDC)

NDC Code	67253-148-45
Package Description	80 mL in 1 BOTTLE (67253-148-45)
Product NDC	67253-148
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amoxicillin
Non-Proprietary Name	Amoxicillin
Dosage Form	POWDER, FOR SUSPENSION
Usage	ORAL
Start Marketing Date	20140801
End Marketing Date	20200229
Marketing Category Name	ANDA
Application Number	ANDA065387
Manufacturer	DAVA Pharmaceuticals Inc
Substance Name	AMOXICILLIN
Strength	250
Strength Unit	mg/5mL
Pharmacy Classes	Penicillin-class Antibacterial [EPC],Penicillins [CS]