Home NDC 69367-615 Salsalate
Product NDC 69367-615
11-digit product format 693670615
Labeler code 69367
Product ID 69367-615_56747829-5049-405d-8d69-83c34d70002b
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Salsalate
Dosage form TABLET
Route ORAL
Labeler Westminster Pharmaceuticals, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2023-11-15
Substance SALSALATE
Active strength 500 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 Salsalate
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALSALATE 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V9MO595C9I Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 312899 Internal RxNorm lookup 583170 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 69367-615-01 Salsalate 100 in 1 BOTTLE TABLET 100 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69367-615 SALSALATE TABLET [WESTMINSTER PHARMACEUTICALS, LLC] 2 Current NDC, 1 package rows 20240209_24815546-658b-4b01-ac11-de7fbd0ebd16.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Salsalate SALSALATE Westminster Pharmaceuticals, LLC 24815546-658b-4b01-ac11-de7fbd0ebd16 2024-02-08 Boxed warning, Warnings, Adverse reactions Exact identifier ndc (product): 69367-615
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69367-615-01 69367061501 100 TABLET in 1 BOTTLE (69367-615-01) 100 tablet 2023-11-15 No No Current