Product NDC: | 11026-2790 |
Proprietary Name: | Broncotron PED |
Non Proprietary Name: | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
Active Ingredient(s): | 5; 100; 2.5 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11026-2790 |
Labeler Name: | Seyer Pharmatec, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121215 |
Package NDC: | 11026-2790-2 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (11026-2790-2) > 60 mL in 1 BOTTLE, DROPPER |
NDC Code | 11026-2790-2 |
Proprietary Name | Broncotron PED |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (11026-2790-2) > 60 mL in 1 BOTTLE, DROPPER |
Product NDC | 11026-2790 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | ORAL |
Start Marketing Date | 20121215 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Seyer Pharmatec, Inc. |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 5; 100; 2.5 |
Strength Unit | mg/5mL; mg/5mL; mg/5mL |
Pharmaceutical Classes |