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Siltussin SA - 54838-117-70 - (Guaifenesin)

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Drug Information of Siltussin SA

Product NDC: 54838-117
Proprietary Name: Siltussin SA
Non Proprietary Name: Guaifenesin
Active Ingredient(s): 100    mg/5mL & nbsp;   Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Siltussin SA

Product NDC: 54838-117
Labeler Name: Silarx Pharmaceuticals, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19981005

Package Information of Siltussin SA

Package NDC: 54838-117-70
Package Description: 237 mL in 1 BOTTLE, PLASTIC (54838-117-70)

NDC Information of Siltussin SA

NDC Code 54838-117-70
Proprietary Name Siltussin SA
Package Description 237 mL in 1 BOTTLE, PLASTIC (54838-117-70)
Product NDC 54838-117
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19981005
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Silarx Pharmaceuticals, Inc
Substance Name GUAIFENESIN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Siltussin SA


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