Product NDC: | 68016-340 |
Proprietary Name: | Premier Value Arthritis Pain Reliever |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 650 mg/1 & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68016-340 |
Labeler Name: | Premier Value |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA078569 |
Marketing Category: | ANDA |
Start Marketing Date: | 20121221 |
Package NDC: | 68016-340-08 |
Package Description: | 80 TABLET, EXTENDED RELEASE in 1 BOTTLE (68016-340-08) |
NDC Code | 68016-340-08 |
Proprietary Name | Premier Value Arthritis Pain Reliever |
Package Description | 80 TABLET, EXTENDED RELEASE in 1 BOTTLE (68016-340-08) |
Product NDC | 68016-340 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20121221 |
Marketing Category Name | ANDA |
Labeler Name | Premier Value |
Substance Name | ACETAMINOPHEN |
Strength Number | 650 |
Strength Unit | mg/1 |
Pharmaceutical Classes |