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RISPERDAL M-TAB
RISPERDAL M-TAB - 50458-315-28 - (risperidone)
Drug Information of RISPERDAL M-TAB
| Product NDC: | 50458-315 |
| Proprietary Name: | RISPERDAL M-TAB |
| Non Proprietary Name: | risperidone |
| Active Ingredient(s): | 1 mg/1 & nbsp; risperidone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of RISPERDAL M-TAB
| Product NDC: | 50458-315 |
| Labeler Name: | Janssen Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021444 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030402 |
Package Information of RISPERDAL M-TAB
| Package NDC: | 50458-315-28 |
| Package Description: | 7 BLISTER PACK in 1 BOX (50458-315-28) > 4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of RISPERDAL M-TAB
| NDC Code | 50458-315-28 |
| Proprietary Name | RISPERDAL M-TAB |
| Package Description | 7 BLISTER PACK in 1 BOX (50458-315-28) > 4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 50458-315 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | risperidone |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20030402 |
| Marketing Category Name | NDA |
| Labeler Name | Janssen Pharmaceuticals, Inc. |
| Substance Name | RISPERIDONE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
