Home
>
National Drug Code (NDC)
>
Sunmark aspirin
Sunmark aspirin - 49348-756-53 - (Aspirin)
Drug Information of Sunmark aspirin
| Product NDC: | 49348-756 |
| Proprietary Name: | Sunmark 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 Sunmark aspirin
| Product NDC: | 49348-756 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20030811 |
Package Information of Sunmark aspirin
| Package NDC: | 49348-756-53 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-756-53) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE |
NDC Information of Sunmark aspirin
| NDC Code | 49348-756-53 |
| Proprietary Name | Sunmark aspirin |
| Package Description | 1 BOTTLE in 1 CARTON (49348-756-53) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE |
| Product NDC | 49348-756 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aspirin |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20030811 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | McKesson |
| Substance Name | ASPIRIN |
| Strength Number | 81 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
