Package 51655-087-52

Brand: alfuzosin hydrochloride

Generic: alfuzosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-087-52
Digits Only 5165508752
Product NDC 51655-087
Product ID 51655-087_46ddcd42-e20f-656c-e063-6294a90a7e5f
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-087-52)

Marketing

Marketing Status
Marketed Since 2022-10-04
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": "46ddcd42-e20f-656c-e063-6294a90a7e5f", "openfda": {"unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["f2a530bd-6a86-251d-e053-2995a90adac4"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-087-52)", "package_ndc": "51655-087-52", "marketing_start_date": "20221004"}], "brand_name": "Alfuzosin Hydrochloride", "product_id": "51655-087_46ddcd42-e20f-656c-e063-6294a90a7e5f", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "51655-087", "generic_name": "Alfuzosin Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "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": "20221004", "listing_expiration_date": "20271231"}