Giltuss - 58552-122-08 - (Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride)

Alphabetical Index


Drug Information of Giltuss

Product NDC: 58552-122
Proprietary Name: Giltuss
Non Proprietary Name: Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
Active Ingredient(s): 28; 388; 10    mg/5mL; mg/5mL; mg/5mL & nbsp;   Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Giltuss

Product NDC: 58552-122
Labeler Name: Gil Pharmaceutical Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20091019

Package Information of Giltuss

Package NDC: 58552-122-08
Package Description: 237 mL in 1 BOTTLE (58552-122-08)

NDC Information of Giltuss

NDC Code 58552-122-08
Proprietary Name Giltuss
Package Description 237 mL in 1 BOTTLE (58552-122-08)
Product NDC 58552-122
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20091019
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Gil Pharmaceutical Corp
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 28; 388; 10
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Giltuss


General Information