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Tusnel DM
Tusnel DM - 54859-603-02 - (Dextromethorphan, Guiafenesin, Pseudoephedrine HCl)
Drug Information of Tusnel DM
| Product NDC: | 54859-603 |
| Proprietary Name: | Tusnel DM |
| Non Proprietary Name: | Dextromethorphan, Guiafenesin, Pseudoephedrine HCl |
| Active Ingredient(s): | 2.5; 25; 7.5 mg/mL; mg/mL; mg/mL & nbsp; Dextromethorphan, Guiafenesin, Pseudoephedrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tusnel DM
| Product NDC: | 54859-603 |
| Labeler Name: | Llorens Pharmaceutical International Division |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19930101 |
Package Information of Tusnel DM
| Package NDC: | 54859-603-02 |
| Package Description: | 60 mL in 1 BOTTLE, DROPPER (54859-603-02) |
NDC Information of Tusnel DM
| NDC Code | 54859-603-02 |
| Proprietary Name | Tusnel DM |
| Package Description | 60 mL in 1 BOTTLE, DROPPER (54859-603-02) |
| Product NDC | 54859-603 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan, Guiafenesin, Pseudoephedrine HCl |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | ORAL |
| Start Marketing Date | 19930101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Llorens Pharmaceutical International Division |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 2.5; 25; 7.5 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
