finasteride

Generic: finasteride

Labeler: thirty madison inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name finasteride
Generic Name finasteride
Labeler thirty madison inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

finasteride 1 mg/1

Manufacturer
Thirty Madison Inc

Identifiers & Regulatory

Product NDC 71713-099
Product ID 71713-099_3fe7bdaa-b027-4da9-94ee-550bf28c63e1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207750
Listing Expiration 2026-12-31
Marketing Start 2021-03-22

Pharmacologic Class

Established (EPC)
5-alpha reductase inhibitor [epc]
Mechanism of Action
5-alpha reductase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71713099
Hyphenated Format 71713-099

Supplemental Identifiers

RxCUI
200172
UNII
57GNO57U7G
NUI
N0000175836 N0000000126

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name finasteride (source: ndc)
Generic Name finasteride (source: ndc)
Application Number ANDA207750 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 CONTAINER (71713-099-90)
source: ndc

Packages (1)

71713-099-90 90 TABLET in 1 CONTAINER (71713-099-90)

Ingredients (1)

finasteride (1 mg/1)

Linked Drug Pages (1)

Finasteride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3fe7bdaa-b027-4da9-94ee-550bf28c63e1", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["3fe7bdaa-b027-4da9-94ee-550bf28c63e1"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Thirty Madison Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 CONTAINER (71713-099-90)", "package_ndc": "71713-099-90", "marketing_start_date": "20210322"}], "brand_name": "Finasteride", "product_id": "71713-099_3fe7bdaa-b027-4da9-94ee-550bf28c63e1", "dosage_form": "TABLET", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "71713-099", "generic_name": "Finasteride", "labeler_name": "Thirty Madison Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "ANDA207750", "marketing_category": "ANDA", "marketing_start_date": "20210322", "listing_expiration_date": "20261231"}