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"71335-0819-3" National Drug Code (NDC)

Lovastatin 60 TABLET in 1 BOTTLE (71335-0819-3)
(Bryant Ranch Prepack)

NDC Code71335-0819-3
Package Description60 TABLET in 1 BOTTLE (71335-0819-3)
Product NDC71335-0819
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
Strength20
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0819-3





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