Package 68788-7981-1

Brand: phenazopyridine hydrochloride

Generic: phenazopyridine
NDC Package

Package Facts

Identity

Package NDC 68788-7981-1
Digits Only 6878879811
Product NDC 68788-7981
Description

15 TABLET in 1 BOTTLE (68788-7981-1)

Marketing

Marketing Status
Marketed Since 2021-07-28
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": "b0cdcdcc-66b2-4a5e-99eb-f63f8ff20103", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094107"], "spl_set_id": ["132cc592-6b03-4b75-bf39-df476fb9dc81"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-7981-1)", "package_ndc": "68788-7981-1", "marketing_start_date": "20210728"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (68788-7981-6)", "package_ndc": "68788-7981-6", "marketing_start_date": "20230825"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "68788-7981_b0cdcdcc-66b2-4a5e-99eb-f63f8ff20103", "dosage_form": "TABLET", "product_ndc": "68788-7981", "generic_name": "Phenazopyridine", "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": "20210728", "listing_expiration_date": "20261231"}