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SALSALATE
SALSALATE - 51862-142-01 - (SALSALATE)
Drug Information of SALSALATE
| Product NDC: | 51862-142 |
| 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: | 51862-142 |
| Labeler Name: | Libertas Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110522 |
Package Information of SALSALATE
| Package NDC: | 51862-142-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (51862-142-01) |
NDC Information of SALSALATE
| NDC Code | 51862-142-01 |
| Proprietary Name | SALSALATE |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (51862-142-01) |
| Product NDC | 51862-142 |
| 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 | Libertas Pharma, Inc. |
| Substance Name | SALSALATE |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
