Home NDC 51655-007 Phenazopyridine Hydrochloride
Product NDC 51655-007
11-digit product format 516550007
Labeler code 51655
Product ID 51655-007_46dd9f29-5a07-f939-e063-6394a90a6768
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Phenazopyridine
Dosage form TABLET
Route ORAL
Labeler Northwind Health Company, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2022-08-05
Substance PHENAZOPYRIDINE HYDROCHLORIDE
Active strength 100 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 100 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 1094107 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 51655-007-27 Phenazopyridine Hydrochloride 12 in 1 BOTTLE, PLASTIC TABLET 12 2 51655-007-53 Phenazopyridine Hydrochloride 10 in 1 BOTTLE, PLASTIC TABLET 10 2 51655-007-87 Phenazopyridine Hydrochloride 6 in 1 BOTTLE, PLASTIC TABLET 6 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51655-007 PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [NORTHWIND PHARMACEUTICALS, LLC] 1 Current NDC, 3 package rows 20230207_f29f2ed6-6fd1-fd65-e053-2a95a90aedc4.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 51655-007-27 51655000727 12 TABLET in 1 BOTTLE, PLASTIC (51655-007-27) 12 tablet 2022-12-19 No No Current 51655-007-53 51655000753 10 TABLET in 1 BOTTLE, PLASTIC (51655-007-53) 10 tablet 2022-11-22 No No Current 51655-007-87 51655000787 6 TABLET in 1 BOTTLE, PLASTIC (51655-007-87) 6 tablet 2022-08-05 No No Current