Salsalate

Product NDC
69367-160
11-digit product format
693670160
Labeler code
69367
Product ID
69367-160_4abdd342-9e7d-4cfa-b7d9-f0e87544f43e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Salsalate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Westminster Pharmaceuticals, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-08-24
Marketing end
0000-00-00
Substance
SALSALATE
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69367-160-04EA - Each69367-1604234ea38-b5c0-4786-92f4-cb05ecf0d06112017-10-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
69367-160-0469367016004100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-160-04) 2017-08-240000-00-00NoNoCurrent