Product NDC: | 52959-018 |
Proprietary Name: | Regular Strength Aspirin EC |
Non Proprietary Name: | Aspirin |
Active Ingredient(s): | 325 mg/1 & nbsp; Aspirin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, DELAYED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52959-018 |
Labeler Name: | H.J. Harkins Company, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110909 |
Package NDC: | 52959-018-80 |
Package Description: | 80 TABLET, DELAYED RELEASE in 1 BOTTLE (52959-018-80) |
NDC Code | 52959-018-80 |
Proprietary Name | Regular Strength Aspirin EC |
Package Description | 80 TABLET, DELAYED RELEASE in 1 BOTTLE (52959-018-80) |
Product NDC | 52959-018 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aspirin |
Dosage Form Name | TABLET, DELAYED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20110909 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | H.J. Harkins Company, Inc. |
Substance Name | ASPIRIN |
Strength Number | 325 |
Strength Unit | mg/1 |
Pharmaceutical Classes |