Home NDC 83324-199-12 Quality Choice Maximum Strength Urinary Pain Relief
Product NDC 83324-199
Requested package NDC 83324-199-12
11-digit product format 833240199
Labeler code 83324
Product ID 83324-199_893a5ae5-858d-4f19-b0d4-d838643e0160
Type HUMAN OTC DRUG
Nonproprietary name PHENAZOPYRIDINE HYDROCHLORIDE
Dosage form TABLET
Route ORAL
Labeler Chain Drug Marketing Association
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-12-02
Substance PHENAZOPYRIDINE HYDROCHLORIDE
Active strength 99.5 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Quality Choice Maximum Strength Urinary Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PHENAZOPYRIDINE HYDROCHLORIDE 99.5 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 1094147 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 83324-199-12 Quality Choice Maximum Strength Urinary Pain Relief 1 in 1 CARTON TABLET 1 1 83324-199-12 Quality Choice Maximum Strength Urinary Pain Relief 12 in 1 BLISTER PACK TABLET 12 1 83324-199-24 Quality Choice Maximum Strength Urinary Pain Relief 24 in 1 BLISTER PACK TABLET 24 1 83324-199-24 Quality Choice Maximum Strength Urinary Pain Relief 1 in 1 CARTON TABLET 1 1
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 83324-199-12 83324019912 1 BLISTER PACK in 1 CARTON (83324-199-12) / 12 TABLET in 1 BLISTER PACK 1 blister pack 2025-12-02 No No Current