Package 50090-6951-0

Brand: phenazopyridine hydrochloride

Generic: phenazopyridine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6951-0
Digits Only 5009069510
Product NDC 50090-6951
Description

9 TABLET in 1 BOTTLE (50090-6951-0)

Marketing

Marketing Status
Marketed Since 2023-12-19
Brand phenazopyridine hydrochloride
Generic phenazopyridine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "89bec0b9-5861-4e39-805d-15160bb819e3", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["d514fd31-feeb-4371-9b28-eec9834a7003"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BOTTLE (50090-6951-0)", "package_ndc": "50090-6951-0", "marketing_start_date": "20231219"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "50090-6951_89bec0b9-5861-4e39-805d-15160bb819e3", "dosage_form": "TABLET", "product_ndc": "50090-6951", "generic_name": "Phenazopyridine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenazopyridine Hydrochloride", "active_ingredients": [{"name": "PHENAZOPYRIDINE HYDROCHLORIDE", "strength": "200 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20231019", "listing_expiration_date": "20261231"}