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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pimozide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PIMOZIDE | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1HIZ4DL86F |
| Rxcui | 198103, 312439 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70954-854-10 | Pimozide | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |