Package 68788-8668-1

Brand: phenazopyridine hydrochloride

Generic: phenazopyridine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8668-1
Digits Only 6878886681
Product NDC 68788-8668
Product ID 68788-8668_97f3acb5-0a37-43d5-a68d-9dfd78c59f1b
Description

15 TABLET in 1 BOTTLE (68788-8668-1)

Marketing

Marketing Status
Marketed Since 2024-05-20
Brand phenazopyridine hydrochloride
Generic phenazopyridine hydrochloride
Sample Package No

Linked Drug Pages (1)

Phenazopyridine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "97f3acb5-0a37-43d5-a68d-9dfd78c59f1b", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094107"], "spl_set_id": ["ce702be2-eec2-4346-965e-f1f6ba342fc9"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-8668-1)", "package_ndc": "68788-8668-1", "marketing_start_date": "20240520"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (68788-8668-6)", "package_ndc": "68788-8668-6", "marketing_start_date": "20240520"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "68788-8668_97f3acb5-0a37-43d5-a68d-9dfd78c59f1b", "dosage_form": "TABLET", "product_ndc": "68788-8668", "generic_name": "Phenazopyridine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenazopyridine Hydrochloride", "active_ingredients": [{"name": "PHENAZOPYRIDINE HYDROCHLORIDE", "strength": "100 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240520", "listing_expiration_date": "20261231"}