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Trifluoperazine Hydrochloride - 0781-1032-01 - (Trifluoperazine Hydrochloride)

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Drug Information of Trifluoperazine Hydrochloride

Product NDC: 0781-1032
Proprietary Name: Trifluoperazine Hydrochloride
Non Proprietary Name: Trifluoperazine Hydrochloride
Active Ingredient(s): 2    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: 0781-1032
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085786
Marketing Category: ANDA
Start Marketing Date: 19811120

Package Information of Trifluoperazine Hydrochloride

Package NDC: 0781-1032-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0781-1032-01)

NDC Information of Trifluoperazine Hydrochloride

NDC Code 0781-1032-01
Proprietary Name Trifluoperazine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0781-1032-01)
Product NDC 0781-1032
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trifluoperazine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19811120
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name TRIFLUOPERAZINE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Trifluoperazine Hydrochloride


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