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Siltussin DM
Siltussin DM - 54838-209-40 - (Guaifenesin and Dextromethorphan Hydrobromide)
Drug Information of Siltussin DM
| Product NDC: | 54838-209 |
| Proprietary Name: | Siltussin DM |
| Non Proprietary Name: | Guaifenesin and Dextromethorphan Hydrobromide |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; Guaifenesin and Dextromethorphan Hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Siltussin DM
| Product NDC: | 54838-209 |
| Labeler Name: | Silarx Pharmaceuticals,Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19920905 |
Package Information of Siltussin DM
| Package NDC: | 54838-209-40 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (54838-209-40) |
NDC Information of Siltussin DM
| NDC Code | 54838-209-40 |
| Proprietary Name | Siltussin DM |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (54838-209-40) |
| Product NDC | 54838-209 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin and Dextromethorphan Hydrobromide |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19920905 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Silarx Pharmaceuticals,Inc |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
