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Ultra Tuss DM
Ultra Tuss DM - 42213-161-93 - (guaifenesin dextromethorphan HBr)
Drug Information of Ultra Tuss DM
| Product NDC: | 42213-161 |
| Proprietary Name: | Ultra Tuss DM |
| Non Proprietary Name: | guaifenesin dextromethorphan HBr |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; guaifenesin dextromethorphan HBr |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultra Tuss DM
| Product NDC: | 42213-161 |
| Labeler Name: | Ultra Seal Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120619 |
Package Information of Ultra Tuss DM
| Package NDC: | 42213-161-93 |
| Package Description: | 474 mL in 1 BOTTLE (42213-161-93) |
NDC Information of Ultra Tuss DM
| NDC Code | 42213-161-93 |
| Proprietary Name | Ultra Tuss DM |
| Package Description | 474 mL in 1 BOTTLE (42213-161-93) |
| Product NDC | 42213-161 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | guaifenesin dextromethorphan HBr |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20120619 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ultra Seal Corporation |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
