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 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7981
Product ID
68788-7981_b0cdcdcc-66b2-4a5e-99eb-f63f8ff20103
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2021-07-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887981
Hyphenated Format
68788-7981
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
- 100 mg/1
Packaging
- 15 TABLET in 1 BOTTLE (68788-7981-1)
- 6 TABLET in 1 BOTTLE (68788-7981-6)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b0cdcdcc-66b2-4a5e-99eb-f63f8ff20103", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094107"], "spl_set_id": ["132cc592-6b03-4b75-bf39-df476fb9dc81"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-7981-1)", "package_ndc": "68788-7981-1", "marketing_start_date": "20210728"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (68788-7981-6)", "package_ndc": "68788-7981-6", "marketing_start_date": "20230825"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "68788-7981_b0cdcdcc-66b2-4a5e-99eb-f63f8ff20103", "dosage_form": "TABLET", "product_ndc": "68788-7981", "generic_name": "Phenazopyridine", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenazopyridine Hydrochloride", "active_ingredients": [{"name": "PHENAZOPYRIDINE HYDROCHLORIDE", "strength": "100 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210728", "listing_expiration_date": "20261231"}