FANAPT
- Product NDC
- 43068-115
- 11-digit product format
- 430680115
- Labeler code
- 43068
- Product ID
- 43068-115_2609a5b3-d7ec-48a9-a32b-54a9b207f9aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ILOPERIDONE
- Dosage form
- KIT
- Route
- ORAL
- Labeler
- Vanda Pharmaceuticals Inc.
- Application
- NDA022192
- Marketing category
- NDA
- Marketing start
- 2025-08-01
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| VPO7KJ050N | ILOPERIDONE | 133454-47-4 | ILOPERIDONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 43068-115-04 | 43068011504 | 1 BLISTER PACK in 1 DOSE PACK (43068-115-04) / 1 KIT in 1 BLISTER PACK | 1 blister pack | 2025-08-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| FANAPT | Vanda Pharmaceuticals Inc. | 2026-05-06 | HUMAN PRESCRIPTION DRUG LABEL | 35 |