Visitor Monitoring Drug Overview: MELLARIL
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Overview

Drug Name: MELLARIL
Active Ingredient(s):
THIORIDAZINE HYDROCHLORIDE
Form(s) and Strength(s) Available:
CONCENTRATE; ORAL  - 100MG/ML
CONCENTRATE; ORAL  - 30MG/ML
TABLET; ORAL  - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
 
You can click on a drug name or application number to view drug details or sort the table by clicking the header columns.
 
Drug Name and FDA Application NumberSort imageDosage Form/RouteStrengthMarketing StatusCompany
MELLARIL
(NDA # 011808) 		CONCENTRATE; ORAL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
30MG/ML
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
15MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
150MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
100MG/ML 		Discontinued NOVARTIS
MELLARIL
(NDA # 011808) 		TABLET; ORAL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
30MG/ML
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
15MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
150MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
100MG/ML 		Discontinued NOVARTIS
©2019 Drugs That Causes a False Positive on a Drug Test