Salsalate

Product NDC
69367-616
11-digit product format
693670616
Labeler code
69367
Product ID
69367-616_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
750 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
IngredientStrength
SALSALATE750 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiV9MO595C9I
Rxcui312899, 583170

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69367-616-01Salsalate100 in 1 BOTTLETABLET1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69367-616SALSALATE TABLET [WESTMINSTER PHARMACEUTICALS, LLC]2Current NDC, 1 package rows20240209_24815546-658b-4b01-ac11-de7fbd0ebd16.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312899salsalate 500 MG Oral TabletPSN24815546-658b-4b01-ac11-de7fbd0ebd162
583170salsalate 750 MG Oral TabletPSN24815546-658b-4b01-ac11-de7fbd0ebd162
312899salsalate 500 MG Oral TabletSCD24815546-658b-4b01-ac11-de7fbd0ebd162
583170salsalate 750 MG Oral TabletSCD24815546-658b-4b01-ac11-de7fbd0ebd162

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69367-616-0169367061601100 TABLET in 1 BOTTLE (69367-616-01) 100 tablet2023-11-15NoNoCurrent