Salsalate - 50682-508-01 - (Salsalate)

Alphabetical Index


Drug Information of Salsalate

Product NDC: 50682-508
Proprietary Name: Salsalate
Non Proprietary Name: Salsalate
Active Ingredient(s): 750    mg/1 & nbsp;   Salsalate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Salsalate

Product NDC: 50682-508
Labeler Name: 3T Federal Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120116

Package Information of Salsalate

Package NDC: 50682-508-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (50682-508-01)

NDC Information of Salsalate

NDC Code 50682-508-01
Proprietary Name Salsalate
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (50682-508-01)
Product NDC 50682-508
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Salsalate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120116
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name 3T Federal Solutions LLC
Substance Name SALSALATE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Salsalate


General Information