Z-TUSS - 58407-239-01 - (Codeine Phosphate/Guaifenesin/Pseudoephedrine Hydrochloride)

Alphabetical Index

Drug Information of Z-TUSS

Product NDC: 58407-239
Proprietary Name: Z-TUSS
Non Proprietary Name: Codeine Phosphate/Guaifenesin/Pseudoephedrine Hydrochloride
Active Ingredient(s): 9; 200; 30    mg/5mL; mg/5mL; mg/5mL & nbsp;   Codeine Phosphate/Guaifenesin/Pseudoephedrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Z-TUSS

Product NDC: 58407-239
Labeler Name: Magna Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20111012

Package Information of Z-TUSS

Package NDC: 58407-239-01
Package Description: 15 mL in 1 BOTTLE, PLASTIC (58407-239-01)

NDC Information of Z-TUSS

NDC Code 58407-239-01
Proprietary Name Z-TUSS
Package Description 15 mL in 1 BOTTLE, PLASTIC (58407-239-01)
Product NDC 58407-239
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Codeine Phosphate/Guaifenesin/Pseudoephedrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20111012
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Magna Pharmaceuticals, Inc.
Strength Number 9; 200; 30
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Z-TUSS

General Information