Home NDC 71335-2321 Phenazopyridine Hydrochloride
Product NDC 71335-2321
11-digit product format 713352321
Labeler code 71335
Product ID 71335-2321_55b0c95f-c150-418a-83a9-1708a517d1f5
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Phenazopyridine Hydrochloride
Dosage form TABLET
Route ORAL
Labeler Bryant Ranch Prepack
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2023-10-19
Substance PHENAZOPYRIDINE HYDROCHLORIDE
Active strength 200 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 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 71335-2321-1 Phenazopyridine Hydrochloride 9 in 1 BOTTLE TABLET 9 101 71335-2321-2 Phenazopyridine Hydrochloride 20 in 1 BOTTLE TABLET 20 101 71335-2321-3 Phenazopyridine Hydrochloride 30 in 1 BOTTLE TABLET 30 101 71335-2321-4 Phenazopyridine Hydrochloride 10 in 1 BOTTLE TABLET 10 101 71335-2321-5 Phenazopyridine Hydrochloride 15 in 1 BOTTLE TABLET 15 101 71335-2321-6 Phenazopyridine Hydrochloride 6 in 1 BOTTLE TABLET 6 101 71335-2321-7 Phenazopyridine Hydrochloride 90 in 1 BOTTLE TABLET 90 101 71335-2321-8 Phenazopyridine Hydrochloride 12 in 1 BOTTLE TABLET 12 101 71335-2321-9 Phenazopyridine Hydrochloride 18 in 1 BOTTLE TABLET 18 101
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71335-2321 PHENAZOPYRIDINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] 101 Current NDC, 9 package rows 20240820_24786685-978b-4485-995a-2964802bc262.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 71335-2321-1 71335232101 9 TABLET in 1 BOTTLE (71335-2321-1) 9 tablet 2024-01-04 No No Current 71335-2321-2 71335232102 20 TABLET in 1 BOTTLE (71335-2321-2) 20 tablet 2024-01-04 No No Current 71335-2321-3 71335232103 30 TABLET in 1 BOTTLE (71335-2321-3) 30 tablet 2024-01-04 No No Current 71335-2321-4 71335232104 10 TABLET in 1 BOTTLE (71335-2321-4) 10 tablet 2024-01-04 No No Current 71335-2321-5 71335232105 15 TABLET in 1 BOTTLE (71335-2321-5) 15 tablet 2024-01-04 No No Current 71335-2321-6 71335232106 6 TABLET in 1 BOTTLE (71335-2321-6) 6 tablet 2024-01-04 No No Current 71335-2321-7 71335232107 90 TABLET in 1 BOTTLE (71335-2321-7) 90 tablet 2024-01-04 No No Current 71335-2321-8 71335232108 12 TABLET in 1 BOTTLE (71335-2321-8) 12 tablet 2024-01-04 No No Current 71335-2321-9 71335232109 18 TABLET in 1 BOTTLE (71335-2321-9) 18 tablet 2024-01-04 No No Current