Product NDC: | 54859-512 |
Proprietary Name: | Dologesic |
Non Proprietary Name: | Acetaminophen, Phenyltoloxamine Citrate, Alcohol |
Active Ingredient(s): | 500; .75; 30 mg/15mL; mL/15mL; mg/15mL & nbsp; Acetaminophen, Phenyltoloxamine Citrate, Alcohol |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54859-512 |
Labeler Name: | Llorens Pharmaceutical International Division |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19940901 |
Package NDC: | 54859-512-06 |
Package Description: | 177 mL in 1 BOTTLE (54859-512-06) |
NDC Code | 54859-512-06 |
Proprietary Name | Dologesic |
Package Description | 177 mL in 1 BOTTLE (54859-512-06) |
Product NDC | 54859-512 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Phenyltoloxamine Citrate, Alcohol |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19940901 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Llorens Pharmaceutical International Division |
Substance Name | ACETAMINOPHEN; ALCOHOL; PHENYLTOLOXAMINE CITRATE |
Strength Number | 500; .75; 30 |
Strength Unit | mg/15mL; mL/15mL; mg/15mL |
Pharmaceutical Classes |