SALSALATE - 43353-771-70 - (SALSALATE)

Alphabetical Index


Drug Information of SALSALATE

Product NDC: 43353-771
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: 43353-771
Labeler Name: Aphena Pharma Solutions - Tennessee, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110522

Package Information of SALSALATE

Package NDC: 43353-771-70
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (43353-771-70)

NDC Information of SALSALATE

NDC Code 43353-771-70
Proprietary Name SALSALATE
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (43353-771-70)
Product NDC 43353-771
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SALSALATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110522
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Aphena Pharma Solutions - Tennessee, Inc.
Substance Name SALSALATE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of SALSALATE


General Information