Home
>
National Drug Code (NDC)
>
Q-Tussin
Q-Tussin - 68788-9081-1 - (Guaifenesin)
Drug Information of Q-Tussin
| Product NDC: | 68788-9081 |
| Proprietary Name: | Q-Tussin |
| 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 Q-Tussin
| Product NDC: | 68788-9081 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19971001 |
Package Information of Q-Tussin
| Package NDC: | 68788-9081-1 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (68788-9081-1) |
NDC Information of Q-Tussin
| NDC Code | 68788-9081-1 |
| Proprietary Name | Q-Tussin |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (68788-9081-1) |
| Product NDC | 68788-9081 |
| 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 | Preferred Pharmaceuticals, Inc |
| Substance Name | GUAIFENESIN |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
