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"68001-214-08" National Drug Code (NDC)

Lovastatin 1000 TABLET in 1 BOTTLE (68001-214-08)
(BluePoint Laboratories)

NDC Code68001-214-08
Package Description1000 TABLET in 1 BOTTLE (68001-214-08)
Product NDC68001-214
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20140210
End Marketing Date20190630
Marketing Category NameANDA
Application NumberANDA075636
ManufacturerBluePoint Laboratories
Substance NameLOVASTATIN
Strength40
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/68001-214-08





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