phenazopyridine hydrochloride

Generic: phenazopyridine

Labeler: verityrx, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenazopyridine hydrochloride
Generic Name phenazopyridine
Labeler verityrx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenazopyridine hydrochloride 200 mg/1

Manufacturer
VERITYRX, LLC

Identifiers & Regulatory

Product NDC 83939-0021
Product ID 83939-0021_427b7010-0678-8eb8-e063-6394a90a7eed
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 839390021
Hyphenated Format 83939-0021

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
  • 1 TABLET in 1 POUCH (83939-0021-1)
  • 50 POUCH in 1 BOX, UNIT-DOSE (83939-0021-2) / 1 TABLET in 1 POUCH
  • 100 POUCH in 1 BOX, UNIT-DOSE (83939-0021-3) / 1 TABLET in 1 POUCH
source: ndc

Packages (3)

83939-0021-1 1 TABLET in 1 POUCH (83939-0021-1) 83939-0021-2 50 POUCH in 1 BOX, UNIT-DOSE (83939-0021-2) / 1 TABLET in 1 POUCH 83939-0021-3 100 POUCH in 1 BOX, UNIT-DOSE (83939-0021-3) / 1 TABLET in 1 POUCH

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": "427b7010-0678-8eb8-e063-6394a90a7eed", "openfda": {"unii": ["0EWG668W17"], "rxcui": ["1094104"], "spl_set_id": ["427b6ffb-3ff1-932f-e063-6394a90ae8b9"], "manufacturer_name": ["VERITYRX, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET in 1 POUCH (83939-0021-1)", "package_ndc": "83939-0021-1", "marketing_start_date": "20251103"}, {"sample": false, "description": "50 POUCH in 1 BOX, UNIT-DOSE (83939-0021-2)  / 1 TABLET in 1 POUCH", "package_ndc": "83939-0021-2", "marketing_start_date": "20251103"}, {"sample": false, "description": "100 POUCH in 1 BOX, UNIT-DOSE (83939-0021-3)  / 1 TABLET in 1 POUCH", "package_ndc": "83939-0021-3", "marketing_start_date": "20251103"}], "brand_name": "Phenazopyridine Hydrochloride", "product_id": "83939-0021_427b7010-0678-8eb8-e063-6394a90a7eed", "dosage_form": "TABLET", "product_ndc": "83939-0021", "generic_name": "Phenazopyridine", "labeler_name": "VERITYRX, LLC", "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"}