Home NDC 72162-2540 Phenazopyridine Hydrochloride
Product NDC 72162-2540
11-digit product format 721622540
Labeler code 72162
Product ID 72162-2540_06b34ac0-9193-4ecc-934a-729ac7e7b7e7
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 Ingredient Strength PHENAZOPYRIDINE HYDROCHLORIDE 200 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 1094104 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72162-2540-1 Phenazopyridine Hydrochloride 100 in 1 BOTTLE TABLET 100 100
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72162-2540-1 72162254001 100 TABLET in 1 BOTTLE (72162-2540-1) 100 tablet 2025-09-19 No No Current