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Diabetic Siltussin DM DAS-Na - 68788-6760-1 - (Guaifenesin and Dextromethorphan Hydrobromide)

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Drug Information of Diabetic Siltussin DM DAS-Na

Product NDC: 68788-6760
Proprietary Name: Diabetic Siltussin DM DAS-Na
Non Proprietary Name: Guaifenesin and Dextromethorphan Hydrobromide
Active Ingredient(s): 10; 100    mg/5mL; mg/5mL & nbsp;   Guaifenesin and Dextromethorphan Hydrobromide
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Diabetic Siltussin DM DAS-Na

Product NDC: 68788-6760
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120725

Package Information of Diabetic Siltussin DM DAS-Na

Package NDC: 68788-6760-1
Package Description: 118 mL in 1 BOTTLE, PLASTIC (68788-6760-1)

NDC Information of Diabetic Siltussin DM DAS-Na

NDC Code 68788-6760-1
Proprietary Name Diabetic Siltussin DM DAS-Na
Package Description 118 mL in 1 BOTTLE, PLASTIC (68788-6760-1)
Product NDC 68788-6760
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin and Dextromethorphan Hydrobromide
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20120725
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Diabetic Siltussin DM DAS-Na


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