Clozapine - 0093-3012-84 - (clozapine)

Alphabetical Index


Drug Information of Clozapine

Product NDC: 0093-3012
Proprietary Name: Clozapine
Non Proprietary Name: clozapine
Active Ingredient(s): 25    mg/1 & nbsp;   clozapine
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Clozapine

Product NDC: 0093-3012
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021590
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120830

Package Information of Clozapine

Package NDC: 0093-3012-84
Package Description: 48 BLISTER PACK in 1 CARTON (0093-3012-84) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0093-3012-19)

NDC Information of Clozapine

NDC Code 0093-3012-84
Proprietary Name Clozapine
Package Description 48 BLISTER PACK in 1 CARTON (0093-3012-84) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0093-3012-19)
Product NDC 0093-3012
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clozapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20120830
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name CLOZAPINE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Clozapine


General Information