Theraflu - 0067-6427-06 - (ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PSEUDOEPHEDRINE HCl)

Alphabetical Index


Drug Information of Theraflu

Product NDC: 0067-6427
Proprietary Name: Theraflu
Non Proprietary Name: ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PSEUDOEPHEDRINE HCl
Active Ingredient(s): 1000; 30; 400; 60    mg/1; mg/1; mg/1; mg/1 & nbsp;   ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PSEUDOEPHEDRINE HCl
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Theraflu

Product NDC: 0067-6427
Labeler Name: Novartis Consumer Health, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100801

Package Information of Theraflu

Package NDC: 0067-6427-06
Package Description: 6 POWDER, FOR SOLUTION in 1 CARTON (0067-6427-06)

NDC Information of Theraflu

NDC Code 0067-6427-06
Proprietary Name Theraflu
Package Description 6 POWDER, FOR SOLUTION in 1 CARTON (0067-6427-06)
Product NDC 0067-6427
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PSEUDOEPHEDRINE HCl
Dosage Form Name POWDER, FOR SOLUTION
Route Name ORAL
Start Marketing Date 20100801
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Novartis Consumer Health, Inc.
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 1000; 30; 400; 60
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Theraflu


General Information