Package 72162-1449-9

Brand: alfuzosin hydrochloride

Generic: alfuzosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1449-9
Digits Only 7216214499
Product NDC 72162-1449
Product ID 72162-1449_6e17789e-5114-40cf-a925-4f40afd1dd42
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1449-9)

Marketing

Marketing Status
Marketed Since 2024-07-16
Brand alfuzosin hydrochloride
Generic alfuzosin hydrochloride
Sample Package No

Linked Drug Pages (1)

Alfuzosin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6e17789e-5114-40cf-a925-4f40afd1dd42", "openfda": {"unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["3a541efa-9eed-4a27-b602-7999fc6f59aa"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1449-9)", "package_ndc": "72162-1449-9", "marketing_start_date": "20240716"}], "brand_name": "Alfuzosin Hydrochloride", "product_id": "72162-1449_6e17789e-5114-40cf-a925-4f40afd1dd42", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "72162-1449", "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"}