"61919-676-71" National Drug Code (NDC)

Lovastatin 100 TABLET in 1 BOTTLE (61919-676-71)
(DIRECT RX)

NDC Code61919-676-71
Package Description100 TABLET in 1 BOTTLE (61919-676-71)
Product NDC61919-676
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20160303
Marketing Category NameANDA
Application NumberANDA075636
ManufacturerDIRECT RX
Substance NameLOVASTATIN
Strength20
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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