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"61786-302-19" National Drug Code (NDC)

Finasteride 90 TABLET, FILM COATED in 1 BOTTLE (61786-302-19)
(REMEDYREPACK INC.)

NDC Code61786-302-19
Package Description90 TABLET, FILM COATED in 1 BOTTLE (61786-302-19)
Product NDC61786-302
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150511
Marketing Category NameANDA
Application NumberANDA090121
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/61786-302-19





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