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Risperidone
Risperidone - 49884-212-55 - (Risperidone)
Drug Information of Risperidone
| Product NDC: | 49884-212 |
| Proprietary Name: | Risperidone |
| Non Proprietary Name: | Risperidone |
| Active Ingredient(s): | .25 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: | 49884-212 |
| Labeler Name: | Par Pharmaceutical Companies, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077494 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090601 |
Package Information of Risperidone
| Package NDC: | 49884-212-55 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (49884-212-55) > 5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-212-52) |
NDC Information of Risperidone
| NDC Code | 49884-212-55 |
| Proprietary Name | Risperidone |
| Package Description | 5 BLISTER PACK in 1 CARTON (49884-212-55) > 5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-212-52) |
| Product NDC | 49884-212 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Risperidone |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20090601 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Companies, Inc. |
| Substance Name | RISPERIDONE |
| Strength Number | .25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
