"55111-172-78" National Drug Code (NDC)

Finasteride 10 BLISTER PACK in 1 CARTON (55111-172-78) / 10 TABLET in 1 BLISTER PACK (55111-172-79)
(Dr. Reddy's Laboratories Limited)

NDC Code55111-172-78
Package Description10 BLISTER PACK in 1 CARTON (55111-172-78) / 10 TABLET in 1 BLISTER PACK (55111-172-79)
Product NDC55111-172
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET
UsageORAL
Start Marketing Date20070228
Marketing Category NameANDA
Application NumberANDA076437
ManufacturerDr. Reddy's Laboratories Limited
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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