tussin - 59779-650-26 - (Guaifenesin)

Alphabetical Index


Drug Information of tussin

Product NDC: 59779-650
Proprietary Name: tussin
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 tussin

Product NDC: 59779-650
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19870715

Package Information of tussin

Package NDC: 59779-650-26
Package Description: 1 BOTTLE in 1 CARTON (59779-650-26) > 118 mL in 1 BOTTLE

NDC Information of tussin

NDC Code 59779-650-26
Proprietary Name tussin
Package Description 1 BOTTLE in 1 CARTON (59779-650-26) > 118 mL in 1 BOTTLE
Product NDC 59779-650
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 19870715
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CVS Pharmacy
Substance Name GUAIFENESIN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of tussin


General Information