"55111-172-05" National Drug Code (NDC)

Finasteride 500 TABLET in 1 BOTTLE (55111-172-05)
(Dr. Reddy's Laboratories Limited)

NDC Code55111-172-05
Package Description500 TABLET in 1 BOTTLE (55111-172-05)
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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