FANAPT - Iloperidone
Navigation: NDC > Supplier starting with: N > NOVARTIS PHARMACEUTICALS CORPORATION| Field | Value |
|---|---|
| NDC Code: | 0078-0600 |
| Proprietary Name: | FANAPT |
| Suffix: | |
| Non-Proprietary Name: | Iloperidone |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 01-10-2009 |
| Category Name: | NDA |
| Application Number: | NDA022192 |
| Labeler: | NOVARTIS PHARMACEUTICALS CORPORATION |
| Substance Name: | ILOPERIDONE |
| Active Numerator Strength: | 10 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Atypical Antipsychotic [EPC] |
| DEA Schedule: |