QTussin - 0603-0857-81 - (Guaifenesin)

Alphabetical Index


Drug Information of QTussin

Product NDC: 0603-0857
Proprietary Name: QTussin
Non Proprietary Name: Guaifenesin
Active Ingredient(s): 100    mg/5mL & nbsp;   Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of QTussin

Product NDC: 0603-0857
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19971001

Package Information of QTussin

Package NDC: 0603-0857-81
Package Description: 237 mL in 1 BOTTLE, PLASTIC (0603-0857-81)

NDC Information of QTussin

NDC Code 0603-0857-81
Proprietary Name QTussin
Package Description 237 mL in 1 BOTTLE, PLASTIC (0603-0857-81)
Product NDC 0603-0857
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19971001
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Qualitest Pharmaceuticals
Substance Name GUAIFENESIN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of QTussin


General Information