Product NDC: | 54859-505 |
Proprietary Name: | Tusnel Diabetic |
Non Proprietary Name: | Dextromethorphan, Guaifenesin |
Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; Dextromethorphan, Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54859-505 |
Labeler Name: | LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20031201 |
Package NDC: | 54859-505-04 |
Package Description: | 118 mL in 1 BOTTLE (54859-505-04) |
NDC Code | 54859-505-04 |
Proprietary Name | Tusnel Diabetic |
Package Description | 118 mL in 1 BOTTLE (54859-505-04) |
Product NDC | 54859-505 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan, Guaifenesin |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20031201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 10; 100 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |