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Thioridazine Hydrochloride - 53489-500-01 - (Thioridazine Hydrochloride)

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Drug Information of Thioridazine Hydrochloride

Product NDC: 53489-500
Proprietary Name: Thioridazine Hydrochloride
Non Proprietary Name: Thioridazine Hydrochloride
Active Ingredient(s): 100    mg/1 & nbsp;   Thioridazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Thioridazine Hydrochloride

Product NDC: 53489-500
Labeler Name: Mutual Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089953
Marketing Category: ANDA
Start Marketing Date: 19881007

Package Information of Thioridazine Hydrochloride

Package NDC: 53489-500-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-01)

NDC Information of Thioridazine Hydrochloride

NDC Code 53489-500-01
Proprietary Name Thioridazine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-01)
Product NDC 53489-500
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Thioridazine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19881007
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical
Substance Name THIORIDAZINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Thioridazine Hydrochloride


General Information