Biocof - 45737-249-16 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine HCL)

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Drug Information of Biocof

Product NDC: 45737-249
Proprietary Name: Biocof
Non Proprietary Name: Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine HCL
Active Ingredient(s): 20; 400; 10    mg/5mL; mg/5mL; mg/5mL & nbsp;   Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine HCL
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Biocof

Product NDC: 45737-249
Labeler Name: Advanced Generic Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120701

Package Information of Biocof

Package NDC: 45737-249-16
Package Description: 473 mL in 1 BOTTLE (45737-249-16)

NDC Information of Biocof

NDC Code 45737-249-16
Proprietary Name Biocof
Package Description 473 mL in 1 BOTTLE (45737-249-16)
Product NDC 45737-249
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine HCL
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20120701
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Advanced Generic Corporation
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 20; 400; 10
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Biocof


General Information