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"70518-0113-0" National Drug Code (NDC)

Lovastatin 90 TABLET in 1 BOTTLE (70518-0113-0)
(REMEDYREPACK INC.)

NDC Code70518-0113-0
Package Description90 TABLET in 1 BOTTLE (70518-0113-0)
Product NDC70518-0113
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20170110
Marketing Category NameANDA
Application NumberANDA075991
ManufacturerREMEDYREPACK INC.
Substance NameLOVASTATIN
Strength20
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/70518-0113-0





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