Tussi Pres - 52083-233-01 - (guaifenesin, phenylephrine hydrochloride, dextromethorphan hydrobromide)

Alphabetical Index


Drug Information of Tussi Pres

Product NDC: 52083-233
Proprietary Name: Tussi Pres
Non Proprietary Name: guaifenesin, phenylephrine hydrochloride, dextromethorphan hydrobromide
Active Ingredient(s): 10; 200; 5    mg/5mL; mg/5mL; mg/5mL & nbsp;   guaifenesin, phenylephrine hydrochloride, dextromethorphan hydrobromide
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Tussi Pres

Product NDC: 52083-233
Labeler Name: Kramer Novis
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110328

Package Information of Tussi Pres

Package NDC: 52083-233-01
Package Description: 30 mL in 1 BOTTLE (52083-233-01)

NDC Information of Tussi Pres

NDC Code 52083-233-01
Proprietary Name Tussi Pres
Package Description 30 mL in 1 BOTTLE (52083-233-01)
Product NDC 52083-233
Product Type Name HUMAN OTC DRUG
Non Proprietary Name guaifenesin, phenylephrine hydrochloride, dextromethorphan hydrobromide
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20110328
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Kramer Novis
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 10; 200; 5
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Tussi Pres


General Information