| Product NDC: | 11026-2675 |
| Proprietary Name: | Panatuss |
| Non Proprietary Name: | Dexbrompheniramine Maleate, Dextromethorphan, Phenylephrine |
| Active Ingredient(s): | 2; 20; 10 mg/5mL; mg/5mL; mg/5mL & nbsp; Dexbrompheniramine Maleate, Dextromethorphan, Phenylephrine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11026-2675 |
| Labeler Name: | Seyer Pharmatec, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20050901 |
| Package NDC: | 11026-2675-4 |
| Package Description: | 118 mL in 1 BOTTLE (11026-2675-4) |
| NDC Code | 11026-2675-4 |
| Proprietary Name | Panatuss |
| Package Description | 118 mL in 1 BOTTLE (11026-2675-4) |
| Product NDC | 11026-2675 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dexbrompheniramine Maleate, Dextromethorphan, Phenylephrine |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20050901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Seyer Pharmatec, Inc. |
| Substance Name | DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 2; 20; 10 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |