Package 59212-200-30

Brand: uroxatral

Generic: alfuzosin hcl
NDC Package

Package Facts

Identity

Package NDC 59212-200-30
Digits Only 5921220030
Product NDC 59212-200
Product ID 59212-200_ffbc758d-7556-4269-8947-baa7ddb88541
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (59212-200-30)

Marketing

Marketing Status
Marketed Since 2019-01-18
Brand uroxatral
Generic alfuzosin hcl
Sample Package No

Linked Drug Pages (1)

Uroxatral ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ffbc758d-7556-4269-8947-baa7ddb88541", "openfda": {"unii": ["75046A1XTN"], "rxcui": ["861132", "861134"], "spl_set_id": ["9fc7f119-f36b-44cf-945d-940160f3afe3"], "manufacturer_name": ["Advanz Pharma (US) Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59212-200-10)", "package_ndc": "59212-200-10", "marketing_start_date": "20130603"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (59212-200-30)", "package_ndc": "59212-200-30", "marketing_start_date": "20190118"}], "brand_name": "Uroxatral", "product_id": "59212-200_ffbc758d-7556-4269-8947-baa7ddb88541", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "59212-200", "generic_name": "Alfuzosin HCl", "labeler_name": "Advanz Pharma (US) Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Uroxatral", "active_ingredients": [{"name": "ALFUZOSIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA021287", "marketing_category": "NDA", "marketing_start_date": "20130603", "listing_expiration_date": "20261231"}