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Risperidone
Risperidone - 58165-030-02 - (Risperidone)
Drug Information of Risperidone
| Product NDC: | 58165-030 |
| Proprietary Name: | Risperidone |
| Non Proprietary Name: | Risperidone |
| Active Ingredient(s): | 1 mg/1 & nbsp; Risperidone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Risperidone
| Product NDC: | 58165-030 |
| Labeler Name: | Ratiopharm Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077784 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100608 |
Package Information of Risperidone
| Package NDC: | 58165-030-02 |
| Package Description: | 500 TABLET, COATED in 1 BOTTLE (58165-030-02) |
NDC Information of Risperidone
| NDC Code | 58165-030-02 |
| Proprietary Name | Risperidone |
| Package Description | 500 TABLET, COATED in 1 BOTTLE (58165-030-02) |
| Product NDC | 58165-030 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Risperidone |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100608 |
| Marketing Category Name | ANDA |
| Labeler Name | Ratiopharm Inc |
| Substance Name | RISPERIDONE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
