finasteride

Generic: finasteride

Labeler: atlantic biologicals corps
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name finasteride
Generic Name finasteride
Labeler atlantic biologicals corps
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

finasteride 5 mg/1

Manufacturer
Atlantic Biologicals Corps

Identifiers & Regulatory

Product NDC 17856-0090
Product ID 17856-0090_385463d5-f3d9-96c0-e063-6294a90ac25e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090121
Listing Expiration 2026-12-31
Marketing Start 2010-05-28

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 178560090
Hyphenated Format 17856-0090

Supplemental Identifiers

RxCUI
310346
UNII
57GNO57U7G
NUI
N0000175836 N0000000126

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 ANDA090121 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 1 TABLET, FILM COATED in 1 POUCH (17856-0090-1)
source: ndc

Packages (1)

17856-0090-1 1 TABLET, FILM COATED in 1 POUCH (17856-0090-1)

Ingredients (1)

finasteride (5 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": "385463d5-f3d9-96c0-e063-6294a90ac25e", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["29e59387-120c-4367-9f87-75cb53b6460d"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Atlantic Biologicals Corps"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET, FILM COATED in 1 POUCH (17856-0090-1)", "package_ndc": "17856-0090-1", "marketing_start_date": "20210111"}], "brand_name": "Finasteride", "product_id": "17856-0090_385463d5-f3d9-96c0-e063-6294a90ac25e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "17856-0090", "generic_name": "finasteride", "labeler_name": "Atlantic Biologicals Corps", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "5 mg/1"}], "application_number": "ANDA090121", "marketing_category": "ANDA", "marketing_start_date": "20100528", "listing_expiration_date": "20261231"}