Salsalate

Product NDC
72162-1569
11-digit product format
721621569
Labeler code
72162
Product ID
72162-1569_0ce84910-58f4-4a8d-ace5-e3a9c5b81865
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Salsalate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2014-10-01
Substance
SALSALATE
Active strength
750 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
V9MO595C9ISALSALATE552-94-3SALSALATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-1569-772162156907120 TABLET in 1 BOTTLE (72162-1569-7) 120 tablet2023-05-16NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Salsalate Tablets, USP 500 mg and 750 mg Rx OnlyBryant Ranch Prepack2023-05-16HUMAN PRESCRIPTION DRUG LABEL100