"71335-0882-3" National Drug Code (NDC)

Lovastatin 90 TABLET in 1 BOTTLE (71335-0882-3)
(Bryant Ranch Prepack)

NDC Code71335-0882-3
Package Description90 TABLET in 1 BOTTLE (71335-0882-3)
Product NDC71335-0882
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20071101
Marketing Category NameANDA
Application NumberANDA078296
ManufacturerBryant Ranch Prepack
Substance NameLOVASTATIN
Strength40
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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