Biocotron - 45737-209-16 - (Dextromethorphan, Guaifenesin)

Alphabetical Index


Drug Information of Biocotron

Product NDC: 45737-209
Proprietary Name: Biocotron
Non Proprietary Name: Dextromethorphan, Guaifenesin
Active Ingredient(s): 10; 100    mg/5mL; mg/5mL & nbsp;   Dextromethorphan, Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Biocotron

Product NDC: 45737-209
Labeler Name: Advanced Generic Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090101

Package Information of Biocotron

Package NDC: 45737-209-16
Package Description: 473 mL in 1 BOTTLE (45737-209-16)

NDC Information of Biocotron

NDC Code 45737-209-16
Proprietary Name Biocotron
Package Description 473 mL in 1 BOTTLE (45737-209-16)
Product NDC 45737-209
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextromethorphan, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Advanced Generic Corporation
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC],Sigma-1 Agonist [EPC],Uncompetitive NMDA Receptor Antagonists [MoA],Sigma-1 Receptor Agonists [MoA]

Complete Information of Biocotron


General Information