Product NDC: | 49483-387 |
Proprietary Name: | aspirin |
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) |
Product NDC: | 49483-387 |
Labeler Name: | Time-Cap Labs, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100628 |
Package NDC: | 49483-387-10 |
Package Description: | 1000 TABLET, COATED in 1 BOTTLE, PLASTIC (49483-387-10) |
NDC Code | 49483-387-10 |
Proprietary Name | aspirin |
Package Description | 1000 TABLET, COATED in 1 BOTTLE, PLASTIC (49483-387-10) |
Product NDC | 49483-387 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | aspirin |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20100628 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Time-Cap Labs, Inc |
Substance Name | ASPIRIN |
Strength Number | 81 |
Strength Unit | mg/1 |
Pharmaceutical Classes |