Haloperidol
- Product NDC
- 0904-6661
- 11-digit product format
- 009046661
- Labeler code
- 0904
- Product ID
- 0904-6661_417d8c81-c958-430f-8a84-75c69b8676cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA077580
- Marketing category
- ANDA
- Marketing start
- 2008-01-03
- Substance
- HALOPERIDOL
- Active strength
- 20 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
- Haloperidol
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HALOPERIDOL | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | J6292F8L3D |
| Rxcui | 197754, 310672, 314035 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-6661-04 | Haloperidol | 1 in 1 BLISTER PACK | TABLET | 1 | | 11 |
| 0904-6661-04 | Haloperidol | 30 in 1 CARTON | TABLET | 30 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-6661 | HALOPERIDOL TABLET [MAJOR PHARMACEUTICALS] | 9 | Current NDC, Legacy NDC, 2 package rows | 20250214_e07f02d4-2768-4978-97ee-23ac52d0b846.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 |
|---|
| 0904-6661-04 | 00904666104 | 30 BLISTER PACK in 1 CARTON (0904-6661-04) / 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2008-01-03 | 0000-00-00 | No | No | Current |