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Perphenazine - 21695-415-60 - (Perphenazine)

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Drug Information of Perphenazine

Product NDC: 21695-415
Proprietary Name: Perphenazine
Non Proprietary Name: Perphenazine
Active Ingredient(s): 8    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: 21695-415
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089685
Marketing Category: ANDA
Start Marketing Date: 20100407

Package Information of Perphenazine

Package NDC: 21695-415-60
Package Description: 60 TABLET, FILM COATED in 1 BLISTER PACK (21695-415-60)

NDC Information of Perphenazine

NDC Code 21695-415-60
Proprietary Name Perphenazine
Package Description 60 TABLET, FILM COATED in 1 BLISTER PACK (21695-415-60)
Product NDC 21695-415
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Perphenazine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100407
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name PERPHENAZINE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Perphenazine


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