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Fanapt
Fanapt - 43068-108-01 - (iloperidone)
Drug Information of Fanapt
| Product NDC: | 43068-108 |
| Proprietary Name: | Fanapt |
| Non Proprietary Name: | iloperidone |
| Active Ingredient(s): | 8 mg/1 & nbsp; iloperidone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fanapt
| Product NDC: | 43068-108 |
| Labeler Name: | Vanda Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022192 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20091001 |
Package Information of Fanapt
| Package NDC: | 43068-108-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (43068-108-01) > 14 TABLET in 1 BOTTLE |
NDC Information of Fanapt
| NDC Code | 43068-108-01 |
| Proprietary Name | Fanapt |
| Package Description | 1 BOTTLE in 1 CARTON (43068-108-01) > 14 TABLET in 1 BOTTLE |
| Product NDC | 43068-108 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | iloperidone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | NDA |
| Labeler Name | Vanda Pharmaceuticals Inc. |
| Substance Name | ILOPERIDONE |
| Strength Number | 8 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
