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QTussin
QTussin - 0603-0857-58 - (Guaifenesin)
Drug Information of QTussin
| Product NDC: | 0603-0857 |
| Proprietary Name: | QTussin |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 100 mg/5mL & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of QTussin
| Product NDC: | 0603-0857 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19971001 |
Package Information of QTussin
| Package NDC: | 0603-0857-58 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (0603-0857-58) |
NDC Information of QTussin
| NDC Code | 0603-0857-58 |
| Proprietary Name | QTussin |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (0603-0857-58) |
| Product NDC | 0603-0857 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19971001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | GUAIFENESIN |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
