Package 30142-756-24

Brand: maximum strength urinary pain relief

Generic: phenazopyridine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 30142-756-24
Digits Only 3014275624
Product NDC 30142-756
Description

1 BLISTER PACK in 1 CARTON (30142-756-24) / 24 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2021-05-01
Brand maximum strength urinary pain relief
Generic phenazopyridine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a4a5f566-eb9e-46d1-b93e-f00d32b796ba", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094147"], "spl_set_id": ["3334e3f6-f57c-45f9-9fa5-5ea3f93d335a"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (30142-756-24)  / 24 TABLET in 1 BLISTER PACK", "package_ndc": "30142-756-24", "marketing_start_date": "20210501"}], "brand_name": "Maximum Strength Urinary Pain Relief", "product_id": "30142-756_a4a5f566-eb9e-46d1-b93e-f00d32b796ba", "dosage_form": "TABLET", "product_ndc": "30142-756", "generic_name": "Phenazopyridine Hydrochloride", "labeler_name": "KROGER COMPANY", "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": "20210501", "listing_expiration_date": "20261231"}