| Product NDC: | 63739-522 |
| Proprietary Name: | aspirin |
| Non Proprietary Name: | aspirin |
| Active Ingredient(s): | 81 mg/1 & nbsp; aspirin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63739-522 |
| Labeler Name: | McKesson Packaging Services Business Unit of McKesson Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121113 |
| Package NDC: | 63739-522-10 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-522-10) > 10 TABLET, COATED in 1 BLISTER PACK |
| NDC Code | 63739-522-10 |
| Proprietary Name | aspirin |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-522-10) > 10 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 63739-522 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | aspirin |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121113 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson Packaging Services Business Unit of McKesson Corporation |
| Substance Name | ASPIRIN |
| Strength Number | 81 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |