FazaClo - 18860-102-01 - (clozapine)

Alphabetical Index


Drug Information of FazaClo

Product NDC: 18860-102
Proprietary Name: FazaClo
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 FazaClo

Product NDC: 18860-102
Labeler Name: Jazz Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021590
Marketing Category: NDA
Start Marketing Date: 20080601

Package Information of FazaClo

Package NDC: 18860-102-01
Package Description: 8 BLISTER PACK in 1 CARTON (18860-102-01) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of FazaClo

NDC Code 18860-102-01
Proprietary Name FazaClo
Package Description 8 BLISTER PACK in 1 CARTON (18860-102-01) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 18860-102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clozapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20080601
Marketing Category Name NDA
Labeler Name Jazz Pharmaceuticals, Inc.
Substance Name CLOZAPINE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of FazaClo


General Information