"0185-0070-60" National Drug Code (NDC)

NDC Code	0185-0070-60
Package Description	60 TABLET in 1 BOTTLE (0185-0070-60)
Product NDC	0185-0070
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lovastatin
Non-Proprietary Name	Lovastatin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20011217
End Marketing Date	20210531
Marketing Category Name	ANDA
Application Number	ANDA075636
Manufacturer	Eon Labs, Inc.
Substance Name	LOVASTATIN
Strength	10
Strength Unit	mg/1
Pharmacy Classes	HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]