Package 68788-8695-1

Brand: phenazopyridine hydrochloride

Generic: phenazopyridine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8695-1
Digits Only 6878886951
Product NDC 68788-8695
Product ID 68788-8695_3682822c-56cf-4662-bc92-ab2dccd755e5
Description

15 TABLET in 1 BOTTLE (68788-8695-1)

Marketing

Marketing Status
Marketed Since 2024-06-11
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": "3682822c-56cf-4662-bc92-ab2dccd755e5", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["96308f8c-66e7-486a-a5c0-ee9a133ad051"], "manufacturer_name": ["Preferred Pharmaceuticals Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-8695-1)", "package_ndc": "68788-8695-1", "marketing_start_date": "20240611"}, {"sample": false, "description": "9 TABLET in 1 BOTTLE (68788-8695-9)", "package_ndc": "68788-8695-9", "marketing_start_date": "20240611"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "68788-8695_3682822c-56cf-4662-bc92-ab2dccd755e5", "dosage_form": "TABLET", "product_ndc": "68788-8695", "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": "200 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240611", "listing_expiration_date": "20261231"}