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Trifluoperazine Hydrochloride - 0378-2401-01 - (trifluoperazine hydrochloride)

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Drug Information of Trifluoperazine Hydrochloride

Product NDC: 0378-2401
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: 0378-2401
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040209
Marketing Category: ANDA
Start Marketing Date: 20120822

Package Information of Trifluoperazine Hydrochloride

Package NDC: 0378-2401-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2401-01)

NDC Information of Trifluoperazine Hydrochloride

NDC Code 0378-2401-01
Proprietary Name Trifluoperazine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2401-01)
Product NDC 0378-2401
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name trifluoperazine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120822
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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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