finasteride
Generic: finasteride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
finasteride
Generic Name
finasteride
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
finasteride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0433
Product ID
71335-0433_965d1a37-d574-4894-b08e-c6f21b882379
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)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350433
Hyphenated Format
71335-0433
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-0433-1)
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0433-2)
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0433-3)
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-0433-4)
- 500 TABLET, FILM COATED in 1 BOTTLE (71335-0433-5)
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-0433-6)
Packages (6)
71335-0433-1
100 TABLET, FILM COATED in 1 BOTTLE (71335-0433-1)
71335-0433-2
30 TABLET, FILM COATED in 1 BOTTLE (71335-0433-2)
71335-0433-3
60 TABLET, FILM COATED in 1 BOTTLE (71335-0433-3)
71335-0433-4
90 TABLET, FILM COATED in 1 BOTTLE (71335-0433-4)
71335-0433-5
500 TABLET, FILM COATED in 1 BOTTLE (71335-0433-5)
71335-0433-6
180 TABLET, FILM COATED in 1 BOTTLE (71335-0433-6)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "965d1a37-d574-4894-b08e-c6f21b882379", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["ef9c0b23-4736-4fb0-862c-c2a4d644e0d6"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0433-1)", "package_ndc": "71335-0433-1", "marketing_start_date": "20211216"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0433-2)", "package_ndc": "71335-0433-2", "marketing_start_date": "20180314"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0433-3)", "package_ndc": "71335-0433-3", "marketing_start_date": "20210127"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0433-4)", "package_ndc": "71335-0433-4", "marketing_start_date": "20180503"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71335-0433-5)", "package_ndc": "71335-0433-5", "marketing_start_date": "20180521"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-0433-6)", "package_ndc": "71335-0433-6", "marketing_start_date": "20241030"}], "brand_name": "Finasteride", "product_id": "71335-0433_965d1a37-d574-4894-b08e-c6f21b882379", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "71335-0433", "generic_name": "finasteride", "labeler_name": "Bryant Ranch Prepack", "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"}