phenazopyridine hydrochloride
Generic: phenazopyridine
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
phenazopyridine hydrochloride
Generic Name
phenazopyridine
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
phenazopyridine hydrochloride 200 mg/1
Manufacturer
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
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
- 200 mg/1
Packaging
- 15 TABLET in 1 BOTTLE (68788-7902-1)
- 9 TABLET in 1 BOTTLE (68788-7902-9)
Packages (2)
Ingredients (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"}