alfuzosin hydrochloride

Generic: alfuzosin hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alfuzosin hydrochloride
Generic Name alfuzosin hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

alfuzosin hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

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
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352578
Hyphenated Format 71335-2578

Supplemental Identifiers

RxCUI
861132
UNII
75046A1XTN

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
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)
source: ndc

Packages (5)

Ingredients (1)

alfuzosin hydrochloride (10 mg/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"}