Clozapine - 0093-7772-93 - (Clozapine)

Alphabetical Index


Drug Information of Clozapine

Product NDC: 0093-7772
Proprietary Name: Clozapine
Non Proprietary Name: Clozapine
Active Ingredient(s): 100    mg/1 & nbsp;   Clozapine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Clozapine

Product NDC: 0093-7772
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074949
Marketing Category: ANDA
Start Marketing Date: 20090918

Package Information of Clozapine

Package NDC: 0093-7772-93
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0093-7772-93) > 1 TABLET in 1 BLISTER PACK (0093-7772-19)

NDC Information of Clozapine

NDC Code 0093-7772-93
Proprietary Name Clozapine
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0093-7772-93) > 1 TABLET in 1 BLISTER PACK (0093-7772-19)
Product NDC 0093-7772
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clozapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090918
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name CLOZAPINE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Clozapine


General Information