Ultra Tuss - 42213-160-93 - (guaifenesin)

Alphabetical Index


Drug Information of Ultra Tuss

Product NDC: 42213-160
Proprietary Name: Ultra Tuss
Non Proprietary Name: guaifenesin
Active Ingredient(s): 100    mg/5mL & nbsp;   guaifenesin
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Ultra Tuss

Product NDC: 42213-160
Labeler Name: Ultra Seal Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120619

Package Information of Ultra Tuss

Package NDC: 42213-160-93
Package Description: 474 mL in 1 BOTTLE (42213-160-93)

NDC Information of Ultra Tuss

NDC Code 42213-160-93
Proprietary Name Ultra Tuss
Package Description 474 mL in 1 BOTTLE (42213-160-93)
Product NDC 42213-160
Product Type Name HUMAN OTC DRUG
Non Proprietary Name guaifenesin
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20120619
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Ultra Seal Corporation
Substance Name GUAIFENESIN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Ultra Tuss


General Information