| Product NDC: | 54859-502 |
| Proprietary Name: | Tusnel |
| Non Proprietary Name: | Dextromethorphan, Guiafenesin, Pseudoephedrine HCl |
| Active Ingredient(s): | 15; 200; 30 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan, Guiafenesin, Pseudoephedrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54859-502 |
| Labeler Name: | Llorens Pharmaceutical International Division |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060101 |
| Package NDC: | 54859-502-10 |
| Package Description: | 3786 mL in 1 BOTTLE (54859-502-10) |
| NDC Code | 54859-502-10 |
| Proprietary Name | Tusnel |
| Package Description | 3786 mL in 1 BOTTLE (54859-502-10) |
| Product NDC | 54859-502 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan, Guiafenesin, Pseudoephedrine HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20060101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Llorens Pharmaceutical International Division |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 15; 200; 30 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |