"49349-531-02" National Drug Code (NDC)

Lovastatin 30 TABLET in 1 BLISTER PACK (49349-531-02)
(REMEDYREPACK INC.)

NDC Code49349-531-02
Package Description30 TABLET in 1 BLISTER PACK (49349-531-02)
Product NDC49349-531
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20110923
Marketing Category NameANDA
Application NumberANDA075828
ManufacturerREMEDYREPACK INC.
Substance NameLOVASTATIN
Strength40
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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