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Aspirin EC
Aspirin EC - 21695-684-90 - (Aspirin)
Drug Information of Aspirin EC
| Product NDC: | 21695-684 |
| Proprietary Name: | Aspirin EC |
| 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) |
Labeler Information of Aspirin EC
| Product NDC: | 21695-684 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19930101 |
Package Information of Aspirin EC
| Package NDC: | 21695-684-90 |
| Package Description: | 90 TABLET, COATED in 1 BOTTLE (21695-684-90) |
NDC Information of Aspirin EC
| NDC Code | 21695-684-90 |
| Proprietary Name | Aspirin EC |
| Package Description | 90 TABLET, COATED in 1 BOTTLE (21695-684-90) |
| Product NDC | 21695-684 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aspirin |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 19930101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | ASPIRIN |
| Strength Number | 81 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
