"63629-1020-8" National Drug Code (NDC)

Lovastatin 800 TABLET in 1 BOTTLE (63629-1020-8)
(Bryant Ranch Prepack)

NDC Code63629-1020-8
Package Description800 TABLET in 1 BOTTLE (63629-1020-8)
Product NDC63629-1020
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
Strength40
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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