Home NDC 50090-5876-1 Phenazopyridine Hydrochloride
Product NDC 50090-5876
Requested package NDC 50090-5876-1
11-digit product format 500905876
Labeler code 50090
Product ID 50090-5876_ab18cf45-4c1d-4d6a-9195-e70ad6e0cd68
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Phenazopyridine
Dosage form TABLET
Route ORAL
Labeler A-S Medication Solutions
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
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.
FDA-Initiated Inactive NDC Indexing# NDC, Effective, Related label table NDC Effective Related label 50090-5876-0 2025-09-05 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-1 2025-09-05 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-4 2025-09-05 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-5 2025-09-05 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-6 2025-09-05 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-7 2025-09-05 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-8 2025-09-05 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-0 2024-01-30 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-1 2024-01-30 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-4 2024-01-30 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-5 2024-01-30 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-6 2024-01-30 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-7 2024-01-30 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only 50090-5876-8 2024-01-30 PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50090-5876-0 Phenazopyridine Hydrochloride 10 in 1 BOTTLE TABLET 10 6 50090-5876-1 Phenazopyridine Hydrochloride 15 in 1 BOTTLE TABLET 15 6 50090-5876-4 Phenazopyridine Hydrochloride 6 in 1 BOTTLE TABLET 6 6 50090-5876-5 Phenazopyridine Hydrochloride 60 in 1 BOTTLE TABLET 60 6 50090-5876-6 Phenazopyridine Hydrochloride 12 in 1 BOTTLE TABLET 12 6 50090-5876-7 Phenazopyridine Hydrochloride 9 in 1 BOTTLE TABLET 9 6 50090-5876-8 Phenazopyridine Hydrochloride 21 in 1 BOTTLE TABLET 21 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50090-5876 PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [A-S MEDICATION SOLUTIONS] 3 Current NDC, Legacy NDC, 7 package rows 20220121_d8155f91-d650-4021-91ee-f3b6c1055a36.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 Marketing end Sample Exclude flag Status 50090-5876-1 50090587601 15 TABLET in 1 BOTTLE (50090-5876-1) 15 tablet 2022-01-20 0000-00-00 No No Current