phenazopyridine hydrochloride

Generic: phenazopyridine

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
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 50090-5876
Product ID 50090-5876_ab18cf45-4c1d-4d6a-9195-e70ad6e0cd68
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2011-02-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905876
Hyphenated Format 50090-5876

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
  • 10 TABLET in 1 BOTTLE (50090-5876-0)
  • 15 TABLET in 1 BOTTLE (50090-5876-1)
  • 6 TABLET in 1 BOTTLE (50090-5876-4)
  • 12 TABLET in 1 BOTTLE (50090-5876-6)
  • 9 TABLET in 1 BOTTLE (50090-5876-7)
  • 21 TABLET in 1 BOTTLE (50090-5876-8)
source: ndc

Packages (6)

50090-5876-0 10 TABLET in 1 BOTTLE (50090-5876-0) 50090-5876-1 15 TABLET in 1 BOTTLE (50090-5876-1) 50090-5876-4 6 TABLET in 1 BOTTLE (50090-5876-4) 50090-5876-6 12 TABLET in 1 BOTTLE (50090-5876-6) 50090-5876-7 9 TABLET in 1 BOTTLE (50090-5876-7) 50090-5876-8 21 TABLET in 1 BOTTLE (50090-5876-8)

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": "ab18cf45-4c1d-4d6a-9195-e70ad6e0cd68", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["d8155f91-d650-4021-91ee-f3b6c1055a36"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (50090-5876-0)", "package_ndc": "50090-5876-0", "marketing_start_date": "20211217"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (50090-5876-1)", "package_ndc": "50090-5876-1", "marketing_start_date": "20220120"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (50090-5876-4)", "package_ndc": "50090-5876-4", "marketing_start_date": "20220120"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE (50090-5876-6)", "package_ndc": "50090-5876-6", "marketing_start_date": "20220120"}, {"sample": false, "description": "9 TABLET in 1 BOTTLE (50090-5876-7)", "package_ndc": "50090-5876-7", "marketing_start_date": "20220120"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (50090-5876-8)", "package_ndc": "50090-5876-8", "marketing_start_date": "20211217"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "50090-5876_ab18cf45-4c1d-4d6a-9195-e70ad6e0cd68", "dosage_form": "TABLET", "product_ndc": "50090-5876", "generic_name": "Phenazopyridine", "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": "20110201", "listing_expiration_date": "20261231"}