Product NDC: | 68391-046 |
Proprietary Name: | Berkley and Jensen Pain Relief |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 500 mg/1 & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, GELATIN COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68391-046 |
Labeler Name: | BJWC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091223 |
Package NDC: | 68391-046-90 |
Package Description: | 500 CAPSULE, GELATIN COATED in 1 BOTTLE (68391-046-90) |
NDC Code | 68391-046-90 |
Proprietary Name | Berkley and Jensen Pain Relief |
Package Description | 500 CAPSULE, GELATIN COATED in 1 BOTTLE (68391-046-90) |
Product NDC | 68391-046 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | CAPSULE, GELATIN COATED |
Route Name | ORAL |
Start Marketing Date | 20091223 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | BJWC |
Substance Name | ACETAMINOPHEN |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes |