Package 71335-2578-5

Brand: alfuzosin hydrochloride

Generic: alfuzosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2578-5
Digits Only 7133525785
Product NDC 71335-2578
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-5)

Marketing

Marketing Status
Marketed Since 2025-02-06
Brand alfuzosin hydrochloride
Generic alfuzosin hydrochloride
Sample Package No

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"}