phenazopyridine hydrochloride
Generic: phenazopyridine hydrochloride
Labeler: preferred pharmaceuticals incDrug Facts
Product Profile
Brand Name
phenazopyridine hydrochloride
Generic Name
phenazopyridine hydrochloride
Labeler
preferred pharmaceuticals inc
Dosage Form
TABLET
Routes
Active Ingredients
phenazopyridine hydrochloride 200 mg/1
Manufacturer
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
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 hydrochloride (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 15 TABLET in 1 BOTTLE (68788-8695-1)
- 9 TABLET in 1 BOTTLE (68788-8695-9)
Packages (2)
Ingredients (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"}