Product NDC: | 57344-080 |
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) |
Product NDC: | 57344-080 |
Labeler Name: | AAA Pharmaceutical, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121215 |
Package NDC: | 57344-080-08 |
Package Description: | 2 BOTTLE, PLASTIC in 1 CARTON (57344-080-08) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
NDC Code | 57344-080-08 |
Proprietary Name | Aspirin |
Package Description | 2 BOTTLE, PLASTIC in 1 CARTON (57344-080-08) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
Product NDC | 57344-080 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ASPIRIN |
Dosage Form Name | TABLET, DELAYED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20121215 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AAA Pharmaceutical, Inc. |
Substance Name | ASPIRIN |
Strength Number | 81 |
Strength Unit | mg/1 |
Pharmaceutical Classes |