| Product NDC: | 68016-336 | 
| Proprietary Name: | Premier Value Arthritis 8 Hour | 
| Non Proprietary Name: | Acetaminophen | 
| Active Ingredient(s): | 650 mg/1 & nbsp; Acetaminophen | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 68016-336 | 
| Labeler Name: | Premier Value | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | ANDA076200 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20020430 | 
| Package NDC: | 68016-336-50 | 
| Package Description: | 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68016-336-50) | 
| NDC Code | 68016-336-50 | 
| Proprietary Name | Premier Value Arthritis 8 Hour | 
| Package Description | 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68016-336-50) | 
| Product NDC | 68016-336 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Acetaminophen | 
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE | 
| Route Name | ORAL | 
| Start Marketing Date | 20020430 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Premier Value | 
| Substance Name | ACETAMINOPHEN | 
| Strength Number | 650 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes |