"68001-213-00" National Drug Code (NDC)

Lovastatin 100 TABLET in 1 BOTTLE (68001-213-00)
(BluePoint Laboratories)

NDC Code68001-213-00
Package Description100 TABLET in 1 BOTTLE (68001-213-00)
Product NDC68001-213
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20140210
End Marketing Date20181031
Marketing Category NameANDA
Application NumberANDA075636
ManufacturerBluePoint Laboratories
Substance NameLOVASTATIN
Strength10
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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