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Perphenazine - 0781-1049-01 - (Perphenazine)

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Drug Information of Perphenazine

Product NDC: 0781-1049
Proprietary Name: Perphenazine
Non Proprietary Name: Perphenazine
Active Ingredient(s): 16    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: 0781-1049
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089686
Marketing Category: ANDA
Start Marketing Date: 19881208

Package Information of Perphenazine

Package NDC: 0781-1049-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0781-1049-01)

NDC Information of Perphenazine

NDC Code 0781-1049-01
Proprietary Name Perphenazine
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0781-1049-01)
Product NDC 0781-1049
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 Sandoz Inc
Substance Name PERPHENAZINE
Strength Number 16
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Perphenazine


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