"72162-1739-0" National Drug Code (NDC)

Lovastatin 1000 TABLET in 1 BOTTLE (72162-1739-0)
(Bryant Ranch Prepack)

NDC Code72162-1739-0
Package Description1000 TABLET in 1 BOTTLE (72162-1739-0)
Product NDC72162-1739
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20021125
Marketing Category NameANDA
Application NumberANDA075991
ManufacturerBryant Ranch Prepack
Substance NameLOVASTATIN
Strength10
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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