phenazopyridine hydrochloride
Generic: phenazopyridine
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
phenazopyridine hydrochloride
Generic Name
phenazopyridine
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
phenazopyridine hydrochloride 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-362
Product ID
72789-362_34185cf5-94da-7039-e063-6394a90a9133
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2011-02-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789362
Hyphenated Format
72789-362
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
phenazopyridine hydrochloride (source: ndc)
Generic Name
phenazopyridine (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 6 TABLET in 1 BOTTLE, PLASTIC (72789-362-06)
Packages (1)
Ingredients (1)
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"}