Broncotron - 11026-2681-4 - (Guaifenesin, Dextromethorphan, Phenyphrine Hydrchloride)

Alphabetical Index


Drug Information of Broncotron

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)

Labeler Information of Broncotron

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 Information of Broncotron

Package NDC: 11026-2681-4
Package Description: 118 mL in 1 BOTTLE (11026-2681-4)

NDC Information of Broncotron

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

Complete Information of Broncotron


General Information