Salsalate - 63629-3783-1 - (Salsalate)

Alphabetical Index


Drug Information of Salsalate

Product NDC: 63629-3783
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: 63629-3783
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19950401

Package Information of Salsalate

Package NDC: 63629-3783-1
Package Description: 60 TABLET in 1 BOTTLE (63629-3783-1)

NDC Information of Salsalate

NDC Code 63629-3783-1
Proprietary Name Salsalate
Package Description 60 TABLET in 1 BOTTLE (63629-3783-1)
Product NDC 63629-3783
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Salsalate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950401
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Bryant Ranch Prepack
Substance Name SALSALATE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Salsalate


General Information