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Siltussin DM - 54838-209-70 - (Guaifenesin and Dextromethorphan Hydrobromide)

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Drug Information of Siltussin DM

Product NDC: 54838-209
Proprietary Name: Siltussin DM
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 Siltussin DM

Product NDC: 54838-209
Labeler Name: Silarx Pharmaceuticals,Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19920905

Package Information of Siltussin DM

Package NDC: 54838-209-70
Package Description: 237 mL in 1 BOTTLE, PLASTIC (54838-209-70)

NDC Information of Siltussin DM

NDC Code 54838-209-70
Proprietary Name Siltussin DM
Package Description 237 mL in 1 BOTTLE, PLASTIC (54838-209-70)
Product NDC 54838-209
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin and Dextromethorphan Hydrobromide
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19920905
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Silarx Pharmaceuticals,Inc
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Siltussin DM


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