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Perphenazine - 0615-3585-39 - (Perphenazine)

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Drug Information of Perphenazine

Product NDC: 0615-3585
Proprietary Name: Perphenazine
Non Proprietary Name: Perphenazine
Active Ingredient(s): 4    mg/1 & nbsp;   Perphenazine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Perphenazine

Product NDC: 0615-3585
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089683
Marketing Category: ANDA
Start Marketing Date: 19881208

Package Information of Perphenazine

Package NDC: 0615-3585-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-3585-39)

NDC Information of Perphenazine

NDC Code 0615-3585-39
Proprietary Name Perphenazine
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-3585-39)
Product NDC 0615-3585
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Perphenazine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19881208
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name PERPHENAZINE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Perphenazine


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