| Product NDC: | 11026-2681 |
| Proprietary Name: | Broncotron |
| Non Proprietary Name: | Guaifenesin, Dextromethorphan, Phenyphrine Hydrchloride |
| Active Ingredient(s): | 20; 200; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; Guaifenesin, Dextromethorphan, Phenyphrine Hydrchloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11026-2681 |
| Labeler Name: | SEYER PHARMATEC, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20071001 |
| Package NDC: | 11026-2681-4 |
| Package Description: | 118 mL in 1 BOTTLE (11026-2681-4) |
| NDC Code | 11026-2681-4 |
| Proprietary Name | Broncotron |
| Package Description | 118 mL in 1 BOTTLE (11026-2681-4) |
| Product NDC | 11026-2681 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin, Dextromethorphan, Phenyphrine Hydrchloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20071001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SEYER PHARMATEC, INC. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 20; 200; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |