Product NDC: | 49483-331 |
Proprietary Name: | Enteric Coated Aspirin |
Non Proprietary Name: | Aspirin |
Active Ingredient(s): | 325 mg/3251 & nbsp; Aspirin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, DELAYED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49483-331 |
Labeler Name: | Time-Cap Labs, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110104 |
Package NDC: | 49483-331-01 |
Package Description: | 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (49483-331-01) |
NDC Code | 49483-331-01 |
Proprietary Name | Enteric Coated Aspirin |
Package Description | 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (49483-331-01) |
Product NDC | 49483-331 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aspirin |
Dosage Form Name | TABLET, DELAYED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20110104 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Time-Cap Labs, Inc |
Substance Name | ASPIRIN |
Strength Number | 325 |
Strength Unit | mg/3251 |
Pharmaceutical Classes |