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Double Tussin Intense Cough Reliever
Double Tussin Intense Cough Reliever - 10956-674-01 - (Dextromethorphan Hydrobromide / Guaifenesin)
Drug Information of Double Tussin Intense Cough Reliever
| Product NDC: | 10956-674 |
| Proprietary Name: | Double Tussin Intense Cough Reliever |
| Non Proprietary Name: | Dextromethorphan Hydrobromide / Guaifenesin |
| Active Ingredient(s): | 20; 300 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 Double Tussin Intense Cough Reliever
| Product NDC: | 10956-674 |
| Labeler Name: | Reese Pharmaceutical Co |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110802 |
Package Information of Double Tussin Intense Cough Reliever
| Package NDC: | 10956-674-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (10956-674-01) > 120 mL in 1 BOTTLE, PLASTIC (10956-674-04) |
NDC Information of Double Tussin Intense Cough Reliever
| NDC Code | 10956-674-01 |
| Proprietary Name | Double Tussin Intense Cough Reliever |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (10956-674-01) > 120 mL in 1 BOTTLE, PLASTIC (10956-674-04) |
| Product NDC | 10956-674 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide / Guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110802 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reese Pharmaceutical Co |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 20; 300 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
