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Risperidone
Risperidone - 62756-702-64 - (Risperidone)
Drug Information of Risperidone
| Product NDC: | 62756-702 |
| Proprietary Name: | Risperidone |
| Non Proprietary Name: | Risperidone |
| Active Ingredient(s): | 2 mg/1 & nbsp; Risperidone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Risperidone
| Product NDC: | 62756-702 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078464 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130413 |
Package Information of Risperidone
| Package NDC: | 62756-702-64 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (62756-702-64) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of Risperidone
| NDC Code | 62756-702-64 |
| Proprietary Name | Risperidone |
| Package Description | 3 BLISTER PACK in 1 CARTON (62756-702-64) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 62756-702 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Risperidone |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20130413 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | RISPERIDONE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
