Package 72789-362-06

Brand: phenazopyridine hydrochloride

Generic: phenazopyridine
NDC Package

Package Facts

Identity

Package NDC 72789-362-06
Digits Only 7278936206
Product NDC 72789-362
Description

6 TABLET in 1 BOTTLE, PLASTIC (72789-362-06)

Marketing

Marketing Status
Marketed Since 2023-11-15
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": "34185cf5-94da-7039-e063-6394a90a9133", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094107"], "spl_set_id": ["1522921b-d6c2-420d-ba0d-39ac16ba8b37"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (72789-362-06)", "package_ndc": "72789-362-06", "marketing_start_date": "20231115"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "72789-362_34185cf5-94da-7039-e063-6394a90a9133", "dosage_form": "TABLET", "product_ndc": "72789-362", "generic_name": "Phenazopyridine", "labeler_name": "PD-Rx 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": "20110201", "listing_expiration_date": "20261231"}