FDA.reportPublic FDA data

Phenazopyridine Hydrochloride

Product NDC
71335-2750
11-digit product format
713352750
Labeler code
71335
Product ID
71335-2750_47073c97-afea-4098-80fb-68d4bd2c6d00
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phenazopyridine
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
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
3c9b98b0-72a5-44c5-a4de-7e950c5176c9Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-2750-1Phenazopyridine Hydrochloride9 in 1 BOTTLETABLET91
71335-2750-2Phenazopyridine Hydrochloride20 in 1 BOTTLETABLET201
71335-2750-3Phenazopyridine Hydrochloride30 in 1 BOTTLETABLET301
71335-2750-4Phenazopyridine Hydrochloride10 in 1 BOTTLETABLET101
71335-2750-5Phenazopyridine Hydrochloride15 in 1 BOTTLETABLET151
71335-2750-6Phenazopyridine Hydrochloride6 in 1 BOTTLETABLET61
71335-2750-7Phenazopyridine Hydrochloride90 in 1 BOTTLETABLET901
71335-2750-8Phenazopyridine Hydrochloride12 in 1 BOTTLETABLET121
71335-2750-9Phenazopyridine Hydrochloride18 in 1 BOTTLETABLET181

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 HydrochloridePHENAZOPYRIDINEBryant Ranch Prepack3c9b98b0-72a5-44c5-a4de-7e950c5176c92025-07-24Adverse reactionsExact identifier
ndc (product): 71335-2750

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1094104phenazopyridine HCl 200 MG Oral TabletPSN3c9b98b0-72a5-44c5-a4de-7e950c5176c91
1094104phenazopyridine hydrochloride 200 MG Oral TabletSCD3c9b98b0-72a5-44c5-a4de-7e950c5176c91

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2750-1713352750019 TABLET in 1 BOTTLE (71335-2750-1) 9 tablet2025-07-24NoNoCurrent
71335-2750-27133527500220 TABLET in 1 BOTTLE (71335-2750-2) 20 tablet2025-07-24NoNoCurrent
71335-2750-37133527500330 TABLET in 1 BOTTLE (71335-2750-3) 30 tablet2025-07-24NoNoCurrent
71335-2750-47133527500410 TABLET in 1 BOTTLE (71335-2750-4) 10 tablet2025-07-24NoNoCurrent
71335-2750-57133527500515 TABLET in 1 BOTTLE (71335-2750-5) 15 tablet2025-07-24NoNoCurrent
71335-2750-6713352750066 TABLET in 1 BOTTLE (71335-2750-6) 6 tablet2025-07-24NoNoCurrent
71335-2750-77133527500790 TABLET in 1 BOTTLE (71335-2750-7) 90 tablet2025-07-24NoNoCurrent
71335-2750-87133527500812 TABLET in 1 BOTTLE (71335-2750-8) 12 tablet2025-07-24NoNoCurrent
71335-2750-97133527500918 TABLET in 1 BOTTLE (71335-2750-9) 18 tablet2025-07-24NoNoCurrent