FDA.reportPublic FDA data

Phenazopyridine Hydrochloride

Product NDC
83939-0021
11-digit product format
839390021
Labeler code
83939
Product ID
83939-0021_427b7010-0678-8eb8-e063-6394a90a7eed
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phenazopyridine
Dosage form
TABLET
Route
ORAL
Labeler
VERITYRX, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2011-02-01
Substance
PHENAZOPYRIDINE HYDROCHLORIDE
Active strength
200 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Phenazopyridine Hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PHENAZOPYRIDINE HYDROCHLORIDE200 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
0EWG668W17Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1094104Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
427b6ffb-3ff1-932f-e063-6394a90ae8b9Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83939-0021-1Phenazopyridine Hydrochloride1 in 1 POUCHTABLET11
83939-0021-2Phenazopyridine Hydrochloride1 in 1 POUCHTABLET11
83939-0021-2Phenazopyridine Hydrochloride50 in 1 BOX, UNIT-DOSETABLET501
83939-0021-3Phenazopyridine Hydrochloride100 in 1 BOX, UNIT-DOSETABLET1001
83939-0021-3Phenazopyridine Hydrochloride1 in 1 POUCHTABLET11

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Phenazopyridine HydrochloridePHENAZOPYRIDINEVERITYRX, LLC427b6ffb-3ff1-932f-e063-6394a90ae8b92025-10-31Adverse reactionsExact identifier
ndc (product): 83939-0021

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1094104phenazopyridine HCl 200 MG Oral TabletPSN427b6ffb-3ff1-932f-e063-6394a90ae8b91
1094104phenazopyridine hydrochloride 200 MG Oral TabletSCD427b6ffb-3ff1-932f-e063-6394a90ae8b91

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83939-0021-1839390021011 TABLET in 1 POUCH (83939-0021-1) 1 tablet2025-11-03NoNoCurrent
83939-0021-28393900210250 POUCH in 1 BOX, UNIT-DOSE (83939-0021-2) / 1 TABLET in 1 POUCH50 pouch2025-11-03NoNoCurrent
83939-0021-383939002103100 POUCH in 1 BOX, UNIT-DOSE (83939-0021-3) / 1 TABLET in 1 POUCH100 pouch2025-11-03NoNoCurrent