Pimozide
- Product NDC
- 70954-854
- 11-digit product format
- 709540854
- Labeler code
- 70954
- Product ID
- 70954-854_5ba22dee-c635-4572-8041-6c25d7c5e22d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pimozide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA219897
- Marketing category
- ANDA
- Marketing start
- 2026-04-21
- Substance
- PIMOZIDE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 1HIZ4DL86F | PIMOZIDE | 2062-78-4 | PIMOZIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70954-854-10 | 70954085410 | 100 TABLET in 1 BOTTLE (70954-854-10) | 100 tablet | 2026-04-21 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pimozide Tablets, USP | ANI Pharmaceuticals, Inc. | Esjay Pharma Private Limited | 2026-05-20 | Human Prescription Drug Label | 2 |