phenazopyridine hydrochloride

Generic: phenazopyridine

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
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenazopyridine hydrochloride 200 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7902
Product ID 68788-7902_fc4684d1-34c4-464b-90cd-e89029407116
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2021-05-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887902
Hyphenated Format 68788-7902

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 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE (68788-7902-1)
  • 9 TABLET in 1 BOTTLE (68788-7902-9)
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": "fc4684d1-34c4-464b-90cd-e89029407116", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["c0e5d32e-075f-4c76-8332-a06560001efe"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-7902-1)", "package_ndc": "68788-7902-1", "marketing_start_date": "20210514"}, {"sample": false, "description": "9 TABLET in 1 BOTTLE (68788-7902-9)", "package_ndc": "68788-7902-9", "marketing_start_date": "20230825"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "68788-7902_fc4684d1-34c4-464b-90cd-e89029407116", "dosage_form": "TABLET", "product_ndc": "68788-7902", "generic_name": "Phenazopyridine", "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": "20210514", "listing_expiration_date": "20261231"}