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FazaClo
FazaClo - 18860-106-10 - (clozapine)
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] |
