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VERSACLOZ
VERSACLOZ - 18860-121-01 - (Clozapine)
Drug Information of VERSACLOZ
| Product NDC: | 18860-121 |
| Proprietary Name: | VERSACLOZ |
| Non Proprietary Name: | Clozapine |
| Active Ingredient(s): | 50 mg/mL & nbsp; Clozapine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VERSACLOZ
| Product NDC: | 18860-121 |
| Labeler Name: | Jazz Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA203479 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130215 |
Package Information of VERSACLOZ
| Package NDC: | 18860-121-01 |
| Package Description: | 1 BOTTLE in 1 BOX (18860-121-01) > 100 mL in 1 BOTTLE |
NDC Information of VERSACLOZ
| NDC Code | 18860-121-01 |
| Proprietary Name | VERSACLOZ |
| Package Description | 1 BOTTLE in 1 BOX (18860-121-01) > 100 mL in 1 BOTTLE |
| Product NDC | 18860-121 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clozapine |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20130215 |
| Marketing Category Name | NDA |
| Labeler Name | Jazz Pharmaceuticals, Inc. |
| Substance Name | CLOZAPINE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
