Home NDC 68016-129 Premier Value Maximum Strength Urinary Pain Relief
Product NDC 68016-129
11-digit product format 680160129
Labeler code 68016
Product ID 68016-129_e7f3b59d-5c67-4057-afd4-40c452653317
Type HUMAN OTC DRUG
Nonproprietary name PHENAZOPYRIDINE HYDROCHLORIDE
Dosage form TABLET
Route ORAL
Labeler Chain Drug Consortium, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2019-07-31
Substance PHENAZOPYRIDINE HYDROCHLORIDE
Active strength 99.5 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 Premier Value 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 68016-129-12 Premier Value Maximum Strength Urinary Pain Relief 1 in 1 CARTON TABLET 1 4 68016-129-12 Premier Value Maximum Strength Urinary Pain Relief 12 in 1 BLISTER PACK TABLET 12 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68016-129 PREMIER VALUE MAXIMUM STRENGTH URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [CHAIN DRUG CONSORTIUM, LLC] 4 Current NDC, Legacy NDC, 2 package rows 20241220_bd7a027f-1175-4f9f-b61d-50bda0feaff2.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 68016-129-12 68016012912 1 BLISTER PACK in 1 CARTON (68016-129-12) / 12 TABLET in 1 BLISTER PACK 1 blister pack 2019-07-31 0000-00-00 No No Current