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Ultra Tuss
Ultra Tuss - 42213-160-93 - (guaifenesin)
Drug Information of Ultra Tuss
| Product NDC: | 42213-160 |
| Proprietary Name: | Ultra Tuss |
| Non Proprietary Name: | guaifenesin |
| Active Ingredient(s): | 100 mg/5mL & nbsp; guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultra Tuss
| Product NDC: | 42213-160 |
| 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
| Package NDC: | 42213-160-93 |
| Package Description: | 474 mL in 1 BOTTLE (42213-160-93) |
NDC Information of Ultra Tuss
| NDC Code | 42213-160-93 |
| Proprietary Name | Ultra Tuss |
| Package Description | 474 mL in 1 BOTTLE (42213-160-93) |
| Product NDC | 42213-160 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | guaifenesin |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20120619 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ultra Seal Corporation |
| Substance Name | GUAIFENESIN |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
