Package 57237-114-01
Brand: alfuzosin hydrochloride
Generic: alfuzosin hydrochloridePackage Facts
Identity
Package NDC
57237-114-01
Digits Only
5723711401
Product NDC
57237-114
Description
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-01)
Marketing
Marketing Status
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": "c759b18f-8985-4b41-852f-2aa423b32748", "openfda": {"unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["43675e9d-a361-4109-9ae1-54d80580fbbd"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-01)", "package_ndc": "57237-114-01", "marketing_start_date": "20120830"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-05)", "package_ndc": "57237-114-05", "marketing_start_date": "20120830"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-90)", "package_ndc": "57237-114-90", "marketing_start_date": "20120830"}], "brand_name": "Alfuzosin Hydrochloride", "product_id": "57237-114_c759b18f-8985-4b41-852f-2aa423b32748", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "57237-114", "generic_name": "Alfuzosin Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "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": "20271231"}