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Dextromethorphan HBr and Guaifenesin - 50383-062-06 - (Dextromethorphan HBr and Guaifenesin)

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Drug Information of Dextromethorphan HBr and Guaifenesin

Product NDC: 50383-062
Proprietary Name: Dextromethorphan HBr and Guaifenesin
Non Proprietary Name: Dextromethorphan HBr and Guaifenesin
Active Ingredient(s): 10; 100    mg/5mL; mg/5mL & nbsp;   Dextromethorphan HBr and Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dextromethorphan HBr and Guaifenesin

Product NDC: 50383-062
Labeler Name: Hi-Tech Pharmacal Co., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120307

Package Information of Dextromethorphan HBr and Guaifenesin

Package NDC: 50383-062-06
Package Description: 4 TRAY in 1 CASE (50383-062-06) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-062-05) > 5 mL in 1 CUP, UNIT-DOSE

NDC Information of Dextromethorphan HBr and Guaifenesin

NDC Code 50383-062-06
Proprietary Name Dextromethorphan HBr and Guaifenesin
Package Description 4 TRAY in 1 CASE (50383-062-06) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-062-05) > 5 mL in 1 CUP, UNIT-DOSE
Product NDC 50383-062
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan HBr and Guaifenesin
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20120307
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Hi-Tech Pharmacal Co., Inc.
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Dextromethorphan HBr and Guaifenesin


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