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, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

alfuzosin hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2146
Product ID 71335-2146_20858b72-0778-46d6-be98-37d913c425b0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079057
Listing Expiration 2026-12-31
Marketing Start 2011-11-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352146
Hyphenated Format 71335-2146

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 ANDA079057 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-1)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-2)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-3)
  • 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-4)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-5)
source: ndc

Packages (5)

71335-2146-1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-1) 71335-2146-2 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-2) 71335-2146-3 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-3) 71335-2146-4 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-4) 71335-2146-5 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-5)

Ingredients (1)

alfuzosin hydrochloride (10 mg/1)

Linked Drug Pages (1)

Alfuzosin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "20858b72-0778-46d6-be98-37d913c425b0", "openfda": {"unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["98fa10c2-7c12-44aa-9112-e2fd6fa71d06"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-1)", "package_ndc": "71335-2146-1", "marketing_start_date": "20240403"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-2)", "package_ndc": "71335-2146-2", "marketing_start_date": "20240403"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-3)", "package_ndc": "71335-2146-3", "marketing_start_date": "20230130"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-4)", "package_ndc": "71335-2146-4", "marketing_start_date": "20240403"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-5)", "package_ndc": "71335-2146-5", "marketing_start_date": "20240403"}], "brand_name": "Alfuzosin Hydrochloride", "product_id": "71335-2146_20858b72-0778-46d6-be98-37d913c425b0", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2146", "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": "ANDA079057", "marketing_category": "ANDA", "marketing_start_date": "20111122", "listing_expiration_date": "20261231"}