FazaClo - 18860-106-10 - (clozapine)

Alphabetical Index


Drug Information of FazaClo

Product NDC: 18860-106
Proprietary Name: FazaClo
Non Proprietary Name: clozapine
Active Ingredient(s): 200    mg/1 & nbsp;   clozapine
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of FazaClo

Product NDC: 18860-106
Labeler Name: Jazz Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021590
Marketing Category: NDA
Start Marketing Date: 20100709

Package Information of FazaClo

Package NDC: 18860-106-10
Package Description: 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (18860-106-10)

NDC Information of FazaClo

NDC Code 18860-106-10
Proprietary Name FazaClo
Package Description 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (18860-106-10)
Product NDC 18860-106
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clozapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20100709
Marketing Category Name NDA
Labeler Name Jazz Pharmaceuticals, Inc.
Substance Name CLOZAPINE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of FazaClo


General Information