NDC 57237-061

Finasteride

Finasteride

Finasteride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Rising Health, Llc. The primary component is Finasteride.

Product ID57237-061_019ae597-49a2-40c1-b87a-e656f9c471fc
NDC57237-061
Product TypeHuman Prescription Drug
Proprietary NameFinasteride
Generic NameFinasteride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2013-11-05
Marketing CategoryANDA / ANDA
Application NumberANDA203687
Labeler NameRising Health, LLC
Substance NameFINASTERIDE
Active Ingredient Strength1 mg/1
Pharm Classes5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 57237-061-30

30 TABLET, FILM COATED in 1 BOTTLE (57237-061-30)
Marketing Start Date2013-11-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57237-061-30 [57237006130]

Finasteride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203687
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-11-05

NDC 57237-061-90 [57237006190]

Finasteride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203687
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-11-05

Drug Details

Active Ingredients

IngredientStrength
FINASTERIDE1 mg/1

OpenFDA Data

SPL SET ID:01b88593-99d3-4dd6-a7b6-5438c15bd7b7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 200172
  • Pharmacological Class

    • 5-alpha Reductase Inhibitor [EPC]
    • 5-alpha Reductase Inhibitors [MoA]

    Medicade Reported Pricing

    57237006190 FINASTERIDE 1 MG TABLET

    Pricing Unit: EA | Drug Type:

    57237006130 FINASTERIDE 1 MG TABLET

    Pricing Unit: EA | Drug Type: