HALOPERIDOL DECANOATE
- Product NDC
- 68001-580
- 11-digit product format
- 680010580
- Labeler code
- 68001
- Product ID
- 68001-580_048557ea-f859-f0f2-e063-6294a90af5ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HALOPERIDOL DECANOATE
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- BluePoint Laboratories
- Application
- ANDA209101
- Marketing category
- ANDA
- Marketing start
- 2023-07-31
- Substance
- HALOPERIDOL DECANOATE
- Active strength
- 50 mg/mL
- 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 DECANOATE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HALOPERIDOL DECANOATE | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | AC20PJ4101 |
| Rxcui | 859871, 1719803, 1719862 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68001-580-41 | HALOPERIDOL DECANOATE | 1 in 1 CARTON | INJECTION | 1 | | 3 |
| 68001-580-41 | HALOPERIDOL DECANOATE | 1 mL in 1 VIAL, SINGLE-DOSE | INJECTION | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68001-580 | HALOPERIDOL DECANOATE INJECTION [BLUEPOINT LABORATORIES] | 3 | Current NDC, 2 package rows | 20230915_f2d14406-2ad4-4c5b-9c24-a026f27b415d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68001-580-41 | 68001058041 | 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-580-41) / 1 mL in 1 VIAL, SINGLE-DOSE | 2023-07-31 | No | No | Historical |