"61919-941-90" National Drug Code (NDC)

Lovastatin 90 TABLET in 1 BOTTLE (61919-941-90)
(Direct_Rx)

NDC Code61919-941-90
Package Description90 TABLET in 1 BOTTLE (61919-941-90)
Product NDC61919-941
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA075991
ManufacturerDirect_Rx
Substance NameLOVASTATIN
Strength40
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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