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Diabetic Tussin DM Maximum Strength
Diabetic Tussin DM Maximum Strength - 61787-064-08 - (Dextromethorphan Hydrobromide and Guaifenesin)
Drug Information of Diabetic Tussin DM Maximum Strength
| Product NDC: | 61787-064 |
| Proprietary Name: | Diabetic Tussin DM Maximum Strength |
| Non Proprietary Name: | Dextromethorphan Hydrobromide and Guaifenesin |
| Active Ingredient(s): | 10; 200 mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide and Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diabetic Tussin DM Maximum Strength
| Product NDC: | 61787-064 |
| Labeler Name: | Health Care Products |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19950703 |
Package Information of Diabetic Tussin DM Maximum Strength
| Package NDC: | 61787-064-08 |
| Package Description: | 1 BOTTLE in 1 BOX (61787-064-08) > 237 mL in 1 BOTTLE |
NDC Information of Diabetic Tussin DM Maximum Strength
| NDC Code | 61787-064-08 |
| Proprietary Name | Diabetic Tussin DM Maximum Strength |
| Package Description | 1 BOTTLE in 1 BOX (61787-064-08) > 237 mL in 1 BOTTLE |
| Product NDC | 61787-064 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide and Guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19950703 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Health Care Products |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 200 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
