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Q Tussin DM - 21695-737-04 - (Dextromethorphan HBr and Guaifenesin)

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Drug Information of Q Tussin DM

Product NDC: 21695-737
Proprietary Name: Q Tussin DM
Non Proprietary Name: Dextromethorphan HBr and Guaifenesin
Active Ingredient(s): 10; 100    mg/5mL; mg/5mL & nbsp;   Dextromethorphan HBr and Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Q Tussin DM

Product NDC: 21695-737
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19950401

Package Information of Q Tussin DM

Package NDC: 21695-737-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC (21695-737-04)

NDC Information of Q Tussin DM

NDC Code 21695-737-04
Proprietary Name Q Tussin DM
Package Description 118 mL in 1 BOTTLE, PLASTIC (21695-737-04)
Product NDC 21695-737
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan HBr and Guaifenesin
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 19950401
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rebel Distributors Corp
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Q Tussin DM


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