| Product NDC: | 60505-0380 |
| Proprietary Name: | Risperidone |
| Non Proprietary Name: | Risperidone |
| Active Ingredient(s): | 1 mg/mL & nbsp; Risperidone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 60505-0380 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077719 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090729 |
| Package NDC: | 60505-0380-1 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (60505-0380-1) > 30 mL in 1 BOTTLE, DROPPER |
| NDC Code | 60505-0380-1 |
| Proprietary Name | Risperidone |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (60505-0380-1) > 30 mL in 1 BOTTLE, DROPPER |
| Product NDC | 60505-0380 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Risperidone |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20090729 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | RISPERIDONE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |