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Tussin Original - 49580-0413-8 - (Robitussin)

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Drug Information of Tussin Original

Product NDC: 49580-0413
Proprietary Name: Tussin Original
Non Proprietary Name: Robitussin
Active Ingredient(s): 100    mg/5mL & nbsp;   Robitussin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Tussin Original

Product NDC: 49580-0413
Labeler Name: Aaron Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090116

Package Information of Tussin Original

Package NDC: 49580-0413-8
Package Description: 237 mL in 1 BOTTLE, PLASTIC (49580-0413-8)

NDC Information of Tussin Original

NDC Code 49580-0413-8
Proprietary Name Tussin Original
Package Description 237 mL in 1 BOTTLE, PLASTIC (49580-0413-8)
Product NDC 49580-0413
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Robitussin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090116
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Aaron Industries, Inc.
Substance Name GUAIFENESIN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Tussin Original


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