Product NDC: | 0615-4554 |
Proprietary Name: | Acetaminophen |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 325 mg/1 & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0615-4554 |
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: | 20100804 |
Package NDC: | 0615-4554-67 |
Package Description: | 60 TABLET in 1 BLISTER PACK (0615-4554-67) |
NDC Code | 0615-4554-67 |
Proprietary Name | Acetaminophen |
Package Description | 60 TABLET in 1 BLISTER PACK (0615-4554-67) |
Product NDC | 0615-4554 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100804 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
Substance Name | ACETAMINOPHEN |
Strength Number | 325 |
Strength Unit | mg/1 |
Pharmaceutical Classes |