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Aspirin
Aspirin - 11534-155-11 - (Aspirin)
Drug Information of Aspirin
| Product NDC: | 11534-155 |
| Proprietary Name: | Aspirin |
| Non Proprietary Name: | Aspirin |
| Active Ingredient(s): | 81 mg/1 & nbsp; Aspirin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aspirin
| Product NDC: | 11534-155 |
| Labeler Name: | Sunrise Pharmaceutical Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100103 |
Package Information of Aspirin
| Package NDC: | 11534-155-11 |
| Package Description: | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-155-11) |
NDC Information of Aspirin
| NDC Code | 11534-155-11 |
| Proprietary Name | Aspirin |
| Package Description | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-155-11) |
| Product NDC | 11534-155 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aspirin |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100103 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sunrise Pharmaceutical Inc |
| Substance Name | ASPIRIN |
| Strength Number | 81 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
