Package 68788-7902-1

Brand: phenazopyridine hydrochloride

Generic: phenazopyridine
NDC Package

Package Facts

Identity

Package NDC 68788-7902-1
Digits Only 6878879021
Product NDC 68788-7902
Description

15 TABLET in 1 BOTTLE (68788-7902-1)

Marketing

Marketing Status
Marketed Since 2021-05-14
Brand phenazopyridine hydrochloride
Generic phenazopyridine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fc4684d1-34c4-464b-90cd-e89029407116", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["c0e5d32e-075f-4c76-8332-a06560001efe"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-7902-1)", "package_ndc": "68788-7902-1", "marketing_start_date": "20210514"}, {"sample": false, "description": "9 TABLET in 1 BOTTLE (68788-7902-9)", "package_ndc": "68788-7902-9", "marketing_start_date": "20230825"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "68788-7902_fc4684d1-34c4-464b-90cd-e89029407116", "dosage_form": "TABLET", "product_ndc": "68788-7902", "generic_name": "Phenazopyridine", "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": "20210514", "listing_expiration_date": "20261231"}