Brontuss - 49963-381-01 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)

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Drug Information of Brontuss

Product NDC: 49963-381
Proprietary Name: Brontuss
Non Proprietary Name: Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Active Ingredient(s): 15; 300; 10    mg/5mL; mg/5mL; mg/5mL & nbsp;   Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Brontuss

Product NDC: 49963-381
Labeler Name: Portal Pharmaceutical
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20111222

Package Information of Brontuss

Package NDC: 49963-381-01
Package Description: 30 mL in 1 BOTTLE (49963-381-01)

NDC Information of Brontuss

NDC Code 49963-381-01
Proprietary Name Brontuss
Package Description 30 mL in 1 BOTTLE (49963-381-01)
Product NDC 49963-381
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20111222
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Portal Pharmaceutical
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 15; 300; 10
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Brontuss


General Information