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"52125-403-02" National Drug Code (NDC)

Finasteride 30 TABLET in 1 VIAL (52125-403-02)
(REMEDYREPACK INC.)

NDC Code52125-403-02
Package Description30 TABLET in 1 VIAL (52125-403-02)
Product NDC52125-403
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET
UsageORAL
Start Marketing Date20130514
Marketing Category NameANDA
Application NumberANDA076437
ManufacturerREMEDYREPACK INC.
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-403-02





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