"70377-002-13" National Drug Code (NDC)

NDC Code	70377-002-13
Package Description	45 TABLET, FILM COATED in 1 BOTTLE (70377-002-13)
Product NDC	70377-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Simvastatin
Non-Proprietary Name	Simvastatin
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20151217
Marketing Category Name	ANDA
Application Number	ANDA078034
Manufacturer	Biocon Pharma Inc,
Substance Name	SIMVASTATIN
Strength	10
Strength Unit	mg/1
Pharmacy Classes	HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]