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Tussin DM
Tussin DM - 68016-018-08 - (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN)
Drug Information of Tussin DM
| Product NDC: | 68016-018 |
| Proprietary Name: | Tussin DM |
| Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tussin DM
| Product NDC: | 68016-018 |
| Labeler Name: | Chain Drug Consortium, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120901 |
Package Information of Tussin DM
| Package NDC: | 68016-018-08 |
| Package Description: | 237 mL in 1 BOTTLE, PLASTIC (68016-018-08) |
NDC Information of Tussin DM
| NDC Code | 68016-018-08 |
| Proprietary Name | Tussin DM |
| Package Description | 237 mL in 1 BOTTLE, PLASTIC (68016-018-08) |
| Product NDC | 68016-018 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Chain Drug Consortium, LLC |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
