Phenazopyridine Hydrochloride

Product NDC: 72789-362
11-digit product format: 727890362
Labeler code: 72789
Product ID: 72789-362_34185cf5-94da-7039-e063-6394a90a9133
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Phenazopyridine
Dosage form: TABLET
Route: ORAL
Labeler: PD-Rx Pharmaceuticals, Inc.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2011-02-01
Substance: PHENAZOPYRIDINE HYDROCHLORIDE
Active strength: 100 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
Ingredient	Strength
PHENAZOPYRIDINE HYDROCHLORIDE	100 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
0EWG668W17	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1094107	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
1522921b-d6c2-420d-ba0d-39ac16ba8b37	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72789-362-06	Phenazopyridine Hydrochloride	6 in 1 BOTTLE, PLASTIC	TABLET	6		16

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72789-362-06	EA - Each	72789-362	05935c42-4665-49bd-94e5-1bd18f519c63	1	2024-01-04

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72789-362	PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PD-RX PHARMACEUTICALS, INC.]	16	Current NDC, 1 package rows	20250503_1522921b-d6c2-420d-ba0d-39ac16ba8b37.zip

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Phenazopyridine Hydrochloride	PHENAZOPYRIDINE	PD-Rx Pharmaceuticals, Inc.	1522921b-d6c2-420d-ba0d-39ac16ba8b37	2025-05-01	Adverse reactions	Exact identifier ndc (product): 72789-362

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
0EWG668W17	PHENAZOPYRIDINE HYDROCHLORIDE	136-40-3	PHENAZOPYRIDINE HYDROCHLORIDE
K2J09EMJ52	PHENAZOPYRIDINE	94-78-0	Phenazopyridine

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1094107	phenazopyridine HCl 100 MG Oral Tablet	PSN	1522921b-d6c2-420d-ba0d-39ac16ba8b37	16
1094107	phenazopyridine hydrochloride 100 MG Oral Tablet	SCD	1522921b-d6c2-420d-ba0d-39ac16ba8b37	16

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
72789-362-06	72789036206	6 TABLET in 1 BOTTLE, PLASTIC (72789-362-06)	6 tablet	2023-11-15	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only	PD-Rx Pharmaceuticals, Inc.	2025-05-01	HUMAN PRESCRIPTION DRUG LABEL	16