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Clozaril
Clozaril - 0078-0127-08 - (clozapine)
Drug Information of Clozaril
| Product NDC: | 0078-0127 |
| Proprietary Name: | Clozaril |
| 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 Clozaril
| Product NDC: | 0078-0127 |
| Labeler Name: | Novartis Pharmaceuticals Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019758 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19890930 |
Package Information of Clozaril
| Package NDC: | 0078-0127-08 |
| Package Description: | 500 TABLET in 1 BOTTLE (0078-0127-08) |
NDC Information of Clozaril
| NDC Code | 0078-0127-08 |
| Proprietary Name | Clozaril |
| Package Description | 500 TABLET in 1 BOTTLE (0078-0127-08) |
| Product NDC | 0078-0127 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clozapine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19890930 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Pharmaceuticals Corporation |
| Substance Name | CLOZAPINE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
