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"78206-152-01" National Drug Code (NDC)

Propecia 30 TABLET, FILM COATED in 1 BOTTLE (78206-152-01)
(Organon LLC)

NDC Code78206-152-01
Package Description30 TABLET, FILM COATED in 1 BOTTLE (78206-152-01)
Product NDC78206-152
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePropecia
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210601
Marketing Category NameNDA
Application NumberNDA020788
ManufacturerOrganon LLC
Substance NameFINASTERIDE
Strength1
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/78206-152-01





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