Home > National Drug Code (NDC) > Perphenazine

Perphenazine - 24236-889-24 - (Perphenazine)

Alphabetical Index


Drug Information of Perphenazine

Product NDC: 24236-889
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: 24236-889
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089686
Marketing Category: ANDA
Start Marketing Date: 20130319

Package Information of Perphenazine

Package NDC: 24236-889-24
Package Description: 200 TABLET, FILM COATED in 1 CANISTER (24236-889-24)

NDC Information of Perphenazine

NDC Code 24236-889-24
Proprietary Name Perphenazine
Package Description 200 TABLET, FILM COATED in 1 CANISTER (24236-889-24)
Product NDC 24236-889
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Perphenazine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130319
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name PERPHENAZINE
Strength Number 16
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Perphenazine


General Information