phenazopyridine hydrochloride

Generic: phenazopyridine hydrochloride

Labeler: preferred pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenazopyridine hydrochloride
Generic Name phenazopyridine hydrochloride
Labeler preferred pharmaceuticals inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenazopyridine hydrochloride 200 mg/1

Manufacturer
Preferred Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 68788-8695
Product ID 68788-8695_3682822c-56cf-4662-bc92-ab2dccd755e5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2024-06-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888695
Hyphenated Format 68788-8695

Supplemental Identifiers

RxCUI
1094104
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 hydrochloride (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE (68788-8695-1)
  • 9 TABLET in 1 BOTTLE (68788-8695-9)
source: ndc

Packages (2)

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": "3682822c-56cf-4662-bc92-ab2dccd755e5", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["96308f8c-66e7-486a-a5c0-ee9a133ad051"], "manufacturer_name": ["Preferred Pharmaceuticals Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-8695-1)", "package_ndc": "68788-8695-1", "marketing_start_date": "20240611"}, {"sample": false, "description": "9 TABLET in 1 BOTTLE (68788-8695-9)", "package_ndc": "68788-8695-9", "marketing_start_date": "20240611"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "68788-8695_3682822c-56cf-4662-bc92-ab2dccd755e5", "dosage_form": "TABLET", "product_ndc": "68788-8695", "generic_name": "Phenazopyridine Hydrochloride", "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": "20240611", "listing_expiration_date": "20261231"}