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Salsalate
Salsalate - 42291-756-01 - (Salsalate)
Drug Information of Salsalate
| Product NDC: | 42291-756 |
| 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: | 42291-756 |
| Labeler Name: | AvKARE, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130517 |
Package Information of Salsalate
| Package NDC: | 42291-756-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (42291-756-01) |
NDC Information of Salsalate
| NDC Code | 42291-756-01 |
| Proprietary Name | Salsalate |
| Package Description | 100 TABLET in 1 BOTTLE (42291-756-01) |
| Product NDC | 42291-756 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Salsalate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130517 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | AvKARE, Inc. |
| Substance Name | SALSALATE |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
