Home
>
National Drug Code (NDC)
>
Ultra Tuss Safe
Ultra Tuss Safe - 42213-162-83 - (guaifenesin dextromethorphan HBr)
Drug Information of Ultra Tuss Safe
| Product NDC: | 42213-162 |
| Proprietary Name: | Ultra Tuss Safe |
| 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 Safe
| Product NDC: | 42213-162 |
| 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 Safe
| Package NDC: | 42213-162-83 |
| Package Description: | 1 BOTTLE in 1 CARTON (42213-162-83) > 119 mL in 1 BOTTLE (42213-162-86) |
NDC Information of Ultra Tuss Safe
| NDC Code | 42213-162-83 |
| Proprietary Name | Ultra Tuss Safe |
| Package Description | 1 BOTTLE in 1 CARTON (42213-162-83) > 119 mL in 1 BOTTLE (42213-162-86) |
| Product NDC | 42213-162 |
| 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 |
