Product NDC: | 51660-336 |
Proprietary Name: | Ohm 8 Hour Pain Reliever/Fever Reducer |
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: | 51660-336 |
Labeler Name: | Ohm Laboratories Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA076200 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020430 |
Package NDC: | 51660-336-50 |
Package Description: | 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51660-336-50) |
NDC Code | 51660-336-50 |
Proprietary Name | Ohm 8 Hour Pain Reliever/Fever Reducer |
Package Description | 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51660-336-50) |
Product NDC | 51660-336 |
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 | Ohm Laboratories Inc. |
Substance Name | ACETAMINOPHEN |
Strength Number | 650 |
Strength Unit | mg/1 |
Pharmaceutical Classes |