"57237-241-60" National Drug Code (NDC)

NDC Code	57237-241-60
Package Description	60 TABLET, FILM COATED in 1 BOTTLE (57237-241-60)
Product NDC	57237-241
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Zidovudine
Non-Proprietary Name	Zidovudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20050919
Marketing Category Name	ANDA
Application Number	ANDA077267
Manufacturer	Citron Pharma LLC
Substance Name	ZIDOVUDINE
Strength	300
Strength Unit	mg/1
Pharmacy Classes	Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]