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"52125-405-19" National Drug Code (NDC)

Lovastatin 90 TABLET in 1 BOTTLE (52125-405-19)
(REMEDYREPACK INC.)

NDC Code52125-405-19
Package Description90 TABLET in 1 BOTTLE (52125-405-19)
Product NDC52125-405
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20140311
End Marketing Date20171122
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/52125-405-19





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