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ECOTRIN
ECOTRIN - 0135-0117-01 - (aspirin)
Drug Information of ECOTRIN
| Product NDC: | 0135-0117 |
| Proprietary Name: | ECOTRIN |
| 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 ECOTRIN
| Product NDC: | 0135-0117 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101112 |
Package Information of ECOTRIN
| Package NDC: | 0135-0117-01 |
| Package Description: | 150 TABLET, COATED in 1 BOTTLE (0135-0117-01) |
NDC Information of ECOTRIN
| NDC Code | 0135-0117-01 |
| Proprietary Name | ECOTRIN |
| Package Description | 150 TABLET, COATED in 1 BOTTLE (0135-0117-01) |
| Product NDC | 0135-0117 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | aspirin |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101112 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | ASPIRIN |
| Strength Number | 81 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
