Salsalate - 10135-493-01 - (Salsalate)

Alphabetical Index


Drug Information of Salsalate

Product NDC: 10135-493
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: 10135-493
Labeler Name: Marlex Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20070401

Package Information of Salsalate

Package NDC: 10135-493-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (10135-493-01)

NDC Information of Salsalate

NDC Code 10135-493-01
Proprietary Name Salsalate
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (10135-493-01)
Product NDC 10135-493
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Salsalate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070401
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Marlex Pharmaceuticals Inc
Substance Name SALSALATE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Salsalate


General Information