Product NDC: | 0615-0564 |
Proprietary Name: | Regular Strength Aspirin EC |
Non Proprietary Name: | Aspirin |
Active Ingredient(s): | 325 mg/1 & nbsp; Aspirin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, DELAYED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0615-0564 |
Labeler Name: | NCS HealthCare of KY, Inc dba Vangard Labs |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110909 |
Package NDC: | 0615-0564-39 |
Package Description: | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-0564-39) |
NDC Code | 0615-0564-39 |
Proprietary Name | Regular Strength Aspirin EC |
Package Description | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-0564-39) |
Product NDC | 0615-0564 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aspirin |
Dosage Form Name | TABLET, DELAYED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20110909 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
Substance Name | ASPIRIN |
Strength Number | 325 |
Strength Unit | mg/1 |
Pharmaceutical Classes |