phenazopyridine hydrochloride

Generic: phenazopyridine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenazopyridine hydrochloride
Generic Name phenazopyridine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenazopyridine hydrochloride 200 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6951
Product ID 50090-6951_89bec0b9-5861-4e39-805d-15160bb819e3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2023-10-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906951
Hyphenated Format 50090-6951

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
  • 9 TABLET in 1 BOTTLE (50090-6951-0)
source: ndc

Packages (1)

50090-6951-0 9 TABLET in 1 BOTTLE (50090-6951-0)

Ingredients (1)

phenazopyridine hydrochloride (200 mg/1)

Linked Drug Pages (1)

Phenazopyridine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "89bec0b9-5861-4e39-805d-15160bb819e3", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["d514fd31-feeb-4371-9b28-eec9834a7003"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BOTTLE (50090-6951-0)", "package_ndc": "50090-6951-0", "marketing_start_date": "20231219"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "50090-6951_89bec0b9-5861-4e39-805d-15160bb819e3", "dosage_form": "TABLET", "product_ndc": "50090-6951", "generic_name": "Phenazopyridine Hydrochloride", "labeler_name": "A-S Medication Solutions", "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": "20231019", "listing_expiration_date": "20261231"}