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 Identifiers#

Field, Values table
FieldValues
Unii0EWG668W17
Rxcui1094104

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

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 tablet2025-11-03NoNoHistorical
83939-0021-28393900210250 POUCH in 1 BOX, UNIT-DOSE (83939-0021-2) / 1 TABLET in 1 POUCH50 pouch2025-11-03NoNoHistorical
83939-0021-383939002103100 POUCH in 1 BOX, UNIT-DOSE (83939-0021-3) / 1 TABLET in 1 POUCH100 pouch2025-11-03NoNoHistorical