Iloperidone
- Product NDC
- 51672-4179
- 11-digit product format
- 516724179
- Labeler code
- 51672
- Product ID
- 51672-4179_6787555e-8a11-481c-b05c-179b0aedcf5c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Iloperidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Taro Pharmaceuticals U.S.A., Inc.
- Application
- ANDA207098
- Marketing category
- ANDA
- Marketing start
- 2019-07-22
- Marketing end
- 0000-00-00
- Substance
- ILOPERIDONE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51672-4179 | ILOPERIDONE TABLET ILOPERIDONE KIT [-SUN PHARMACEUTICAL INDUSTRIES, INC.] | 4 | Legacy NDC | 20250406_6f17cc91-86b3-42e3-9bf2-935dd360c3eb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51672-4179-4 | 51672417904 | 60 TABLET in 1 BOTTLE (51672-4179-4) | 60 tablet | 2019-07-22 | 0000-00-00 | No | No | Current |