TUSICOF - 52083-239-16 - (dextromethorphan, guaifenesin, and phenylephrine)

Alphabetical Index


Drug Information of TUSICOF

Product NDC: 52083-239
Proprietary Name: TUSICOF
Non Proprietary Name: dextromethorphan, guaifenesin, and phenylephrine
Active Ingredient(s): 20; 400; 10    mg/5mL; mg/5mL; mg/5mL & nbsp;   dextromethorphan, guaifenesin, and phenylephrine
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of TUSICOF

Product NDC: 52083-239
Labeler Name: Kramer Novis
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100817

Package Information of TUSICOF

Package NDC: 52083-239-16
Package Description: 474 mL in 1 BOTTLE (52083-239-16)

NDC Information of TUSICOF

NDC Code 52083-239-16
Proprietary Name TUSICOF
Package Description 474 mL in 1 BOTTLE (52083-239-16)
Product NDC 52083-239
Product Type Name HUMAN OTC DRUG
Non Proprietary Name dextromethorphan, guaifenesin, and phenylephrine
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20100817
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Kramer Novis
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 20; 400; 10
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of TUSICOF


General Information