Visitor Monitoring Drug Overview: MELLARIL
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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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TABLET; ORAL  - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET; ORAL  - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
 
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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CONCENTRATE; ORAL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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200MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
15MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
150MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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TABLET; ORAL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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
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