Salsalate - 54569-1712-4 - (Salsalate)

Alphabetical Index


Drug Information of Salsalate

Product NDC: 54569-1712
Proprietary Name: Salsalate
Non Proprietary Name: Salsalate
Active Ingredient(s): 750    mg/1 & nbsp;   Salsalate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Salsalate

Product NDC: 54569-1712
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100924

Package Information of Salsalate

Package NDC: 54569-1712-4
Package Description: 30 TABLET in 1 BOTTLE (54569-1712-4)

NDC Information of Salsalate

NDC Code 54569-1712-4
Proprietary Name Salsalate
Package Description 30 TABLET in 1 BOTTLE (54569-1712-4)
Product NDC 54569-1712
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Salsalate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100924
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name A-S Medication Solutions LLC
Substance Name SALSALATE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Salsalate


General Information