"68001-315-08" National Drug Code (NDC)

Lovastatin 1000 TABLET in 1 BOTTLE (68001-315-08)
(BluePoint Laboratories)

NDC Code68001-315-08
Package Description1000 TABLET in 1 BOTTLE (68001-315-08)
Product NDC68001-315
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20071101
Marketing Category NameANDA
Application NumberANDA078296
ManufacturerBluePoint Laboratories
Substance NameLOVASTATIN
Strength20
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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