| Product NDC: | 51596-001 |
| Proprietary Name: | Aspirin to Go |
| Non Proprietary Name: | aspirin |
| Active Ingredient(s): | 325 mg/1 & nbsp; aspirin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51596-001 |
| Labeler Name: | Breakthrough Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101215 |
| Package NDC: | 51596-001-01 |
| Package Description: | 1 POWDER in 1 POUCH (51596-001-01) |
| NDC Code | 51596-001-01 |
| Proprietary Name | Aspirin to Go |
| Package Description | 1 POWDER in 1 POUCH (51596-001-01) |
| Product NDC | 51596-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | aspirin |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20101215 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Breakthrough Products, Inc. |
| Substance Name | ASPIRIN |
| Strength Number | 325 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |