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Dologesic
Dologesic - 54859-110-10 - (Acetaminophen, Phenyltoloxamine Citrate)
Drug Information of Dologesic
| Product NDC: | 54859-110 |
| Proprietary Name: | Dologesic |
| Non Proprietary Name: | Acetaminophen, Phenyltoloxamine Citrate |
| Active Ingredient(s): | 500; 30 mg/1; mg/1 & nbsp; Acetaminophen, Phenyltoloxamine Citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dologesic
| Product NDC: | 54859-110 |
| Labeler Name: | LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090901 |
Package Information of Dologesic
| Package NDC: | 54859-110-10 |
| Package Description: | 100 TABLET in 1 BOTTLE (54859-110-10) |
NDC Information of Dologesic
| NDC Code | 54859-110-10 |
| Proprietary Name | Dologesic |
| Package Description | 100 TABLET in 1 BOTTLE (54859-110-10) |
| Product NDC | 54859-110 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Phenyltoloxamine Citrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION |
| Substance Name | ACETAMINOPHEN; PHENYLTOLOXAMINE CITRATE |
| Strength Number | 500; 30 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
