phenazopyridine hydrochloride

Generic: phenazopyridine

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenazopyridine hydrochloride
Generic Name phenazopyridine
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenazopyridine hydrochloride 200 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-288
Product ID 72789-288_2e6f3b44-0998-8b14-e063-6294a90afb14
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 72789288
Hyphenated Format 72789-288

Supplemental Identifiers

RxCUI
1094104
UPC
0372789288093
UNII
0EWG668W17

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 9 TABLET in 1 BOTTLE, PLASTIC (72789-288-09)
source: ndc

Packages (1)

Ingredients (1)

phenazopyridine hydrochloride (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e6f3b44-0998-8b14-e063-6294a90afb14", "openfda": {"upc": ["0372789288093"], "unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["c1591037-62f4-469f-8bb2-a82e49dfbecf"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BOTTLE, PLASTIC (72789-288-09)", "package_ndc": "72789-288-09", "marketing_start_date": "20221118"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "72789-288_2e6f3b44-0998-8b14-e063-6294a90afb14", "dosage_form": "TABLET", "product_ndc": "72789-288", "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": "200 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20110201", "listing_expiration_date": "20261231"}