Product NDC: | 59779-249 |
Proprietary Name: | Uncoated Aspirin |
Non Proprietary Name: | Aspirin |
Active Ingredient(s): | 325 mg/1 & nbsp; Aspirin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-249 |
Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19930804 |
Package NDC: | 59779-249-16 |
Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (59779-249-16) |
NDC Code | 59779-249-16 |
Proprietary Name | Uncoated Aspirin |
Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (59779-249-16) |
Product NDC | 59779-249 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aspirin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19930804 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
Substance Name | ASPIRIN |
Strength Number | 325 |
Strength Unit | mg/1 |
Pharmaceutical Classes |