Haloperidol
- Product NDC
- 0832-1560
- 11-digit product format
- 008321560
- Labeler code
- 0832
- Product ID
- 0832-1560_326f5ed0-bc46-a1f5-e063-6394a90af2c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories, LLC
- Application
- ANDA211061
- Marketing category
- ANDA
- Marketing start
- 2020-01-09
- Substance
- HALOPERIDOL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Haloperidol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HALOPERIDOL | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | J6292F8L3D |
| Rxcui | 197754, 310670, 310671, 310672, 314034, 314035 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0832-1560-11 | Haloperidol | 100 in 1 BOTTLE | TABLET | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0832-1560 | HALOPERIDOL TABLET [UPSHER-SMITH LABORATORIES, LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250419_afb3ac3e-7459-42d3-b5ca-e0d6d27ced73.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0832-1560-11 | 00832156011 | 100 TABLET in 1 BOTTLE (0832-1560-11) | 100 tablet | 2020-01-13 | 0000-00-00 | No | No | Current |