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Trifluoperazine Hydrochloride - 52125-118-02 - (TRIFLUOPERAZINE HYDROCHLORIDE)

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Drug Information of Trifluoperazine Hydrochloride

Product NDC: 52125-118
Proprietary Name: Trifluoperazine Hydrochloride
Non Proprietary Name: TRIFLUOPERAZINE HYDROCHLORIDE
Active Ingredient(s): 5    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: 52125-118
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040209
Marketing Category: ANDA
Start Marketing Date: 20120927

Package Information of Trifluoperazine Hydrochloride

Package NDC: 52125-118-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-118-02)

NDC Information of Trifluoperazine Hydrochloride

NDC Code 52125-118-02
Proprietary Name Trifluoperazine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-118-02)
Product NDC 52125-118
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRIFLUOPERAZINE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120927
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name TRIFLUOPERAZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Trifluoperazine Hydrochloride


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