Biobron - 45737-246-16 - (Dextromethorphan, Guaifenesin, Phenylephrine)

Alphabetical Index


Drug Information of Biobron

Product NDC: 45737-246
Proprietary Name: Biobron
Non Proprietary Name: Dextromethorphan, Guaifenesin, Phenylephrine
Active Ingredient(s): 20; 200; 10    mg/5mL; mg/5mL; mg/5mL & nbsp;   Dextromethorphan, Guaifenesin, Phenylephrine
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Biobron

Product NDC: 45737-246
Labeler Name: Advanced Generic Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20091001

Package Information of Biobron

Package NDC: 45737-246-16
Package Description: 473 mL in 1 BOTTLE (45737-246-16)

NDC Information of Biobron

NDC Code 45737-246-16
Proprietary Name Biobron
Package Description 473 mL in 1 BOTTLE (45737-246-16)
Product NDC 45737-246
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan, Guaifenesin, Phenylephrine
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20091001
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Advanced Generic Corporation
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 20; 200; 10
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Biobron


General Information