Product NDC: | 55312-440 |
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: | 55312-440 |
Labeler Name: | Western Family Foods, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120104 |
Package NDC: | 55312-440-12 |
Package Description: | 1 BOTTLE in 1 CARTON (55312-440-12) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE |
NDC Code | 55312-440-12 |
Proprietary Name | Aspirin |
Package Description | 1 BOTTLE in 1 CARTON (55312-440-12) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE |
Product NDC | 55312-440 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aspirin |
Dosage Form Name | TABLET, DELAYED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20120104 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Western Family Foods, Inc. |
Substance Name | ASPIRIN |
Strength Number | 81 |
Strength Unit | mg/1 |
Pharmaceutical Classes |