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Tussin Original - 70253-020-04 - (GUAIFENESIN)

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Drug Information of Tussin Original

Product NDC: 70253-020
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: 70253-020
Labeler Name: Nash-Finch Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090320

Package Information of Tussin Original

Package NDC: 70253-020-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC (70253-020-04)

NDC Information of Tussin Original

NDC Code 70253-020-04
Proprietary Name Tussin Original
Package Description 118 mL in 1 BOTTLE, PLASTIC (70253-020-04)
Product NDC 70253-020
Product Type Name HUMAN OTC DRUG
Non Proprietary Name GUAIFENESIN
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090320
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Nash-Finch Company
Substance Name GUAIFENESIN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Tussin Original


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