Bionatuss - 45737-210-16 - (Dexbrompheniramine Maleate, Dextromethorphan, Phenylephrine)

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Drug Information of Bionatuss

Product NDC: 45737-210
Proprietary Name: Bionatuss
Non Proprietary Name: Dexbrompheniramine Maleate, Dextromethorphan, Phenylephrine
Active Ingredient(s): 2; 20; 10    mg/5mL; mg/5mL; mg/5mL & nbsp;   Dexbrompheniramine Maleate, Dextromethorphan, Phenylephrine
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Bionatuss

Product NDC: 45737-210
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 Bionatuss

Package NDC: 45737-210-16
Package Description: 473 mL in 1 BOTTLE (45737-210-16)

NDC Information of Bionatuss

NDC Code 45737-210-16
Proprietary Name Bionatuss
Package Description 473 mL in 1 BOTTLE (45737-210-16)
Product NDC 45737-210
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dexbrompheniramine Maleate, Dextromethorphan, 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 DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 2; 20; 10
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Bionatuss


General Information