Salsalate

Product NDC
42937-703
11-digit product format
429370703
Labeler code
42937
Product ID
42937-703_2357c10f-19f4-4225-b765-640c98ee90f5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Salsalate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Nationwide Laboratories, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2011-08-19
Marketing end
0000-00-00
Substance
SALSALATE
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42937-703-20EA - Each42937-70375f06a18-4be6-4f19-8312-8457fc5a94da12014-07-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
42937-703-1042937070310100 TABLET, FILM COATED in 1 BOTTLE (42937-703-10) 2011-08-190000-00-00NoNoCurrent
42937-703-1642937070316250 TABLET, FILM COATED in 1 BOTTLE (42937-703-16) 2011-08-190000-00-00NoNoCurrent
42937-703-1842937070318500 TABLET, FILM COATED in 1 BOTTLE (42937-703-18) 2011-08-190000-00-00NoNoCurrent
42937-703-20429370703201000 TABLET, FILM COATED in 1 BOTTLE (42937-703-20) 2011-08-190000-00-00NoNoCurrent