Salsalate

Product NDC
42192-366
11-digit product format
421920366
Labeler code
42192
Product ID
42192-366_8c3e426a-26ca-3f7c-e053-2a95a90ae751
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Salsalate
Dosage form
TABLET
Route
ORAL
Labeler
Acella Pharmaceuticals, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2014-03-31
Marketing end
0000-00-00
Substance
SALSALATE
Active strength
750 mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42192-366-10EA - Each42192-36630d51814-24ae-41a2-a280-d52d317af43e12014-08-01

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
42192-366-1042192036610100 TABLET in 1 BOTTLE (42192-366-10) 100 tablet2014-03-310000-00-00NoNoCurrent