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Fluphenazine Hydrochloride - 0615-3574-39 - (Fluphenazine Hydrochloride)

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Drug Information of Fluphenazine Hydrochloride

Product NDC: 0615-3574
Proprietary Name: Fluphenazine Hydrochloride
Non Proprietary Name: Fluphenazine Hydrochloride
Active Ingredient(s): 10    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: 0615-3574
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089804
Marketing Category: ANDA
Start Marketing Date: 19880812

Package Information of Fluphenazine Hydrochloride

Package NDC: 0615-3574-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-3574-39)

NDC Information of Fluphenazine Hydrochloride

NDC Code 0615-3574-39
Proprietary Name Fluphenazine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-3574-39)
Product NDC 0615-3574
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluphenazine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19880812
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name FLUPHENAZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Fluphenazine Hydrochloride


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