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) |
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 NDC: | 50682-508-10 |
Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (50682-508-10) |
NDC Code | 50682-508-10 |
Proprietary Name | Salsalate |
Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (50682-508-10) |
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 |