alfuzosin hydrochloride
Generic: alfuzosin hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
alfuzosin hydrochloride
Generic Name
alfuzosin hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Routes
Active Ingredients
alfuzosin hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2578
Product ID
71335-2578_fc13629f-baf7-427b-ba50-43659558af75
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079060
Listing Expiration
2026-12-31
Marketing Start
2012-08-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352578
Hyphenated Format
71335-2578
Supplemental Identifiers
RxCUI
UNII
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
alfuzosin hydrochloride (source: ndc)
Generic Name
alfuzosin hydrochloride (source: ndc)
Application Number
ANDA079060 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-1)
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-2)
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-3)
- 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-4)
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-5)
Packages (5)
71335-2578-1
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-1)
71335-2578-2
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-2)
71335-2578-3
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-3)
71335-2578-4
120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-4)
71335-2578-5
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fc13629f-baf7-427b-ba50-43659558af75", "openfda": {"unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["37e89394-af6e-4700-bfa8-2effba1a286b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-1)", "package_ndc": "71335-2578-1", "marketing_start_date": "20250206"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-2)", "package_ndc": "71335-2578-2", "marketing_start_date": "20250206"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-3)", "package_ndc": "71335-2578-3", "marketing_start_date": "20250206"}, {"sample": false, "description": "120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-4)", "package_ndc": "71335-2578-4", "marketing_start_date": "20250206"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-5)", "package_ndc": "71335-2578-5", "marketing_start_date": "20250206"}], "brand_name": "Alfuzosin Hydrochloride", "product_id": "71335-2578_fc13629f-baf7-427b-ba50-43659558af75", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2578", "generic_name": "Alfuzosin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alfuzosin Hydrochloride", "active_ingredients": [{"name": "ALFUZOSIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA079060", "marketing_category": "ANDA", "marketing_start_date": "20120830", "listing_expiration_date": "20261231"}