Package 80513-517-72

Brand: maximum strength urinary pain relief

Generic: phenazopyridine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80513-517-72
Digits Only 8051351772
Product NDC 80513-517
Product ID 80513-517_1b87f423-20e1-743e-e063-6294a90aaa03
Description

72 TABLET in 1 BOTTLE (80513-517-72)

Marketing

Marketing Status
Marketed Since 2024-05-01
Brand maximum strength urinary pain relief
Generic phenazopyridine hydrochloride
Sample Package No

Linked Drug Pages (1)

Maximum Strength Urinary Pain Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b87f423-20e1-743e-e063-6294a90aaa03", "openfda": {"upc": ["0380513001047"], "unii": ["0EWG668W17"], "rxcui": ["1094147"], "spl_set_id": ["a10464cf-36b2-460f-b31c-2e0edee3e4cf"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET in 1 BOTTLE (80513-517-72)", "package_ndc": "80513-517-72", "marketing_start_date": "20240501"}], "brand_name": "Maximum Strength Urinary Pain Relief", "product_id": "80513-517_1b87f423-20e1-743e-e063-6294a90aaa03", "dosage_form": "TABLET", "product_ndc": "80513-517", "generic_name": "Phenazopyridine Hydrochloride", "labeler_name": "Advanced Rx LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum Strength Urinary Pain Relief", "active_ingredients": [{"name": "PHENAZOPYRIDINE HYDROCHLORIDE", "strength": "99.5 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}