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Trifluoperazine Hydrochloride - 51079-572-20 - (trifluoperazine hydrochloride)

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Drug Information of Trifluoperazine Hydrochloride

Product NDC: 51079-572
Proprietary Name: Trifluoperazine Hydrochloride
Non Proprietary Name: trifluoperazine hydrochloride
Active Ingredient(s): 1    mg/1 & nbsp;   trifluoperazine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Trifluoperazine Hydrochloride

Product NDC: 51079-572
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040209
Marketing Category: ANDA
Start Marketing Date: 20120105

Package Information of Trifluoperazine Hydrochloride

Package NDC: 51079-572-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-572-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-572-01)

NDC Information of Trifluoperazine Hydrochloride

NDC Code 51079-572-20
Proprietary Name Trifluoperazine Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-572-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-572-01)
Product NDC 51079-572
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name trifluoperazine 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 TRIFLUOPERAZINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Trifluoperazine Hydrochloride


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