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Thioridazine Hydrochloride - 51079-566-20 - (thioridazine hydrochloride)

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Drug Information of Thioridazine Hydrochloride

Product NDC: 51079-566
Proprietary Name: Thioridazine Hydrochloride
Non Proprietary Name: thioridazine hydrochloride
Active Ingredient(s): 25    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: 51079-566
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088004
Marketing Category: ANDA
Start Marketing Date: 20120105

Package Information of Thioridazine Hydrochloride

Package NDC: 51079-566-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-566-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-566-01)

NDC Information of Thioridazine Hydrochloride

NDC Code 51079-566-20
Proprietary Name Thioridazine Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-566-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-566-01)
Product NDC 51079-566
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name thioridazine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120105
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name THIORIDAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Thioridazine Hydrochloride


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