finasteride

Generic: finasteride

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name finasteride
Generic Name finasteride
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

finasteride 1 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-526
Product ID 31722-526_0ebbabf3-0681-484d-ab8d-58e670d80a0d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090060
Listing Expiration 2026-12-31
Marketing Start 2013-07-01

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 31722526
Hyphenated Format 31722-526

Supplemental Identifiers

RxCUI
200172
UPC
0331722526104 0331722526906 0331722526302
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 ANDA090060 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (31722-526-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (31722-526-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (31722-526-90)
source: ndc

Packages (3)

31722-526-10 1000 TABLET, FILM COATED in 1 BOTTLE (31722-526-10) 31722-526-30 30 TABLET, FILM COATED in 1 BOTTLE (31722-526-30) 31722-526-90 90 TABLET, FILM COATED in 1 BOTTLE (31722-526-90)

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": "0ebbabf3-0681-484d-ab8d-58e670d80a0d", "openfda": {"nui": ["N0000175836", "N0000000126"], "upc": ["0331722526104", "0331722526906", "0331722526302"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["00e934bb-c15b-490a-a852-839689a1231a"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (31722-526-10)", "package_ndc": "31722-526-10", "marketing_start_date": "20130701"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-526-30)", "package_ndc": "31722-526-30", "marketing_start_date": "20130701"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-526-90)", "package_ndc": "31722-526-90", "marketing_start_date": "20130701"}], "brand_name": "Finasteride", "product_id": "31722-526_0ebbabf3-0681-484d-ab8d-58e670d80a0d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "31722-526", "generic_name": "Finasteride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "ANDA090060", "marketing_category": "ANDA", "marketing_start_date": "20130701", "listing_expiration_date": "20261231"}