Tussin CF - 56062-516-34 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)

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Drug Information of Tussin CF

Product NDC: 56062-516
Proprietary Name: Tussin CF
Non Proprietary Name: Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Active Ingredient(s): 10; 100; 5    mg/5mL; mg/5mL; mg/5mL & nbsp;   Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Tussin CF

Product NDC: 56062-516
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19930319

Package Information of Tussin CF

Package NDC: 56062-516-34
Package Description: 1 BOTTLE in 1 CARTON (56062-516-34) > 237 mL in 1 BOTTLE

NDC Information of Tussin CF

NDC Code 56062-516-34
Proprietary Name Tussin CF
Package Description 1 BOTTLE in 1 CARTON (56062-516-34) > 237 mL in 1 BOTTLE
Product NDC 56062-516
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19930319
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Publix Super Markets Inc
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 10; 100; 5
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Tussin CF


General Information