| Product NDC: | 11673-416 |
| Proprietary Name: | Up and Up aspirin |
| Non Proprietary Name: | Aspirin |
| Active Ingredient(s): | 325 mg/1 & nbsp; Aspirin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11673-416 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090610 |
| Package NDC: | 11673-416-90 |
| Package Description: | 500 TABLET in 1 BOTTLE (11673-416-90) |
| NDC Code | 11673-416-90 |
| Proprietary Name | Up and Up aspirin |
| Package Description | 500 TABLET in 1 BOTTLE (11673-416-90) |
| Product NDC | 11673-416 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aspirin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090610 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Target Corporation |
| Substance Name | ASPIRIN |
| Strength Number | 325 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |