"49349-982-20" National Drug Code (NDC)

Lovastatin 100 TABLET in 1 VIAL (49349-982-20)
(REMEDYREPACK INC.)

NDC Code49349-982-20
Package Description100 TABLET in 1 VIAL (49349-982-20)
Product NDC49349-982
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20130521
Marketing Category NameANDA
Application NumberANDA075991
ManufacturerREMEDYREPACK INC.
Substance NameLOVASTATIN
Strength10
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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