Home NDC 72789-288-30 Phenazopyridine Hydrochloride
Product NDC 72789-288
Requested package NDC 72789-288-30
11-digit product format 727890288
Labeler code 72789
Product ID 72789-288_5da4940c-8b3d-649c-e063-6294a90a8171
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 200 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
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 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PHENAZOPYRIDINE HYDROCHLORIDE 200 mg/1
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72789-288-09 Phenazopyridine Hydrochloride 9 in 1 BOTTLE, PLASTIC TABLET 9 15
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72789-288 PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PD-RX PHARMACEUTICALS, INC.] 15 Current NDC, Legacy NDC, 1 package rows 20250221_c1591037-62f4-469f-8bb2-a82e49dfbecf.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 72789-288-30 72789028830 30 TABLET in 1 BOTTLE, PLASTIC (72789-288-30) 30 tablet 2026-10-12 No No Current