Home
>
National Drug Code (NDC)
>
Q Tussin DM
Q Tussin DM - 21695-737-04 - (Dextromethorphan HBr and Guaifenesin)
Drug Information of Q Tussin DM
| Product NDC: | 21695-737 |
| Proprietary Name: | Q Tussin DM |
| Non Proprietary Name: | Dextromethorphan HBr and Guaifenesin |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; Dextromethorphan HBr and Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Q Tussin DM
| Product NDC: | 21695-737 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19950401 |
Package Information of Q Tussin DM
| Package NDC: | 21695-737-04 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (21695-737-04) |
NDC Information of Q Tussin DM
| NDC Code | 21695-737-04 |
| Proprietary Name | Q Tussin DM |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (21695-737-04) |
| Product NDC | 21695-737 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan HBr and Guaifenesin |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 19950401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
