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Perphenazine - 67046-541-30 - (Perphenazine)

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Drug Information of Perphenazine

Product NDC: 67046-541
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: 67046-541
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089685
Marketing Category: ANDA
Start Marketing Date: 20100407

Package Information of Perphenazine

Package NDC: 67046-541-30
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-541-30)

NDC Information of Perphenazine

NDC Code 67046-541-30
Proprietary Name Perphenazine
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-541-30)
Product NDC 67046-541
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 Contract Pharmacy Services-PA
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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