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Tussin Original - 59779-310-34 - (GUAIFENESIN)

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Drug Information of Tussin Original

Product NDC: 59779-310
Proprietary Name: Tussin Original
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 Tussin Original

Product NDC: 59779-310
Labeler Name: CVS
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090716

Package Information of Tussin Original

Package NDC: 59779-310-34
Package Description: 237 mL in 1 BOTTLE, PLASTIC (59779-310-34)

NDC Information of Tussin Original

NDC Code 59779-310-34
Proprietary Name Tussin Original
Package Description 237 mL in 1 BOTTLE, PLASTIC (59779-310-34)
Product NDC 59779-310
Product Type Name HUMAN OTC DRUG
Non Proprietary Name GUAIFENESIN
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090716
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CVS
Substance Name GUAIFENESIN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Tussin Original


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