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Fluphenazine Hydrochloride - 0781-1436-10 - (Fluphenazine Hydrochloride)

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Drug Information of Fluphenazine Hydrochloride

Product NDC: 0781-1436
Proprietary Name: Fluphenazine Hydrochloride
Non Proprietary Name: Fluphenazine Hydrochloride
Active Ingredient(s): 1    mg/1 & nbsp;   Fluphenazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fluphenazine Hydrochloride

Product NDC: 0781-1436
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089583
Marketing Category: ANDA
Start Marketing Date: 19871016

Package Information of Fluphenazine Hydrochloride

Package NDC: 0781-1436-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1436-10)

NDC Information of Fluphenazine Hydrochloride

NDC Code 0781-1436-10
Proprietary Name Fluphenazine Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1436-10)
Product NDC 0781-1436
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluphenazine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19871016
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name FLUPHENAZINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Fluphenazine Hydrochloride


General Information