finasteride

Generic: finasteride

Labeler: dr. reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name finasteride
Generic Name finasteride
Labeler dr. reddy's laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

finasteride 5 mg/1

Manufacturer
Dr. Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-172
Product ID 55111-172_3e2181d6-f6be-c77e-e3f3-63e26fc35897
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076437
Listing Expiration 2026-12-31
Marketing Start 2007-02-28

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 55111172
Hyphenated Format 55111-172

Supplemental Identifiers

RxCUI
310346
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 ANDA076437 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (55111-172-01)
  • 500 TABLET in 1 BOTTLE (55111-172-05)
  • 30 TABLET in 1 BOTTLE (55111-172-30)
  • 10 BLISTER PACK in 1 CARTON (55111-172-78) / 10 TABLET in 1 BLISTER PACK (55111-172-79)
  • 90 TABLET in 1 BOTTLE (55111-172-90)
source: ndc

Packages (5)

55111-172-01 100 TABLET in 1 BOTTLE (55111-172-01) 55111-172-05 500 TABLET in 1 BOTTLE (55111-172-05) 55111-172-30 30 TABLET in 1 BOTTLE (55111-172-30) 55111-172-78 10 BLISTER PACK in 1 CARTON (55111-172-78) / 10 TABLET in 1 BLISTER PACK (55111-172-79) 55111-172-90 90 TABLET in 1 BOTTLE (55111-172-90)

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": "3e2181d6-f6be-c77e-e3f3-63e26fc35897", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["a4dd6d6c-c8c7-16a9-aa68-aa46283dfae1"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55111-172-01)", "package_ndc": "55111-172-01", "marketing_start_date": "20070228"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-172-05)", "package_ndc": "55111-172-05", "marketing_start_date": "20070228"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (55111-172-30)", "package_ndc": "55111-172-30", "marketing_start_date": "20070228"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-172-78)  / 10 TABLET in 1 BLISTER PACK (55111-172-79)", "package_ndc": "55111-172-78", "marketing_start_date": "20070228"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (55111-172-90)", "package_ndc": "55111-172-90", "marketing_start_date": "20070228"}], "brand_name": "Finasteride", "product_id": "55111-172_3e2181d6-f6be-c77e-e3f3-63e26fc35897", "dosage_form": "TABLET", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "55111-172", "generic_name": "Finasteride", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "5 mg/1"}], "application_number": "ANDA076437", "marketing_category": "ANDA", "marketing_start_date": "20070228", "listing_expiration_date": "20261231"}