haloperidol
- Product NDC
- 25021-806
- 11-digit product format
- 250210806
- Labeler code
- 25021
- Product ID
- 25021-806_0ee8e325-6089-44b2-8882-055e1c1e3474
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- haloperidol lactate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA091637
- Marketing category
- ANDA
- Marketing start
- 2011-10-24
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL LACTATE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 25021-806 | HALOPERIDOL (HALOPERIDOL LACTATE) INJECTION, SOLUTION [SAGENT PHARMACEUTICALS] | 17 | Legacy NDC | 20250406_7ce7f23c-f58b-4b8b-a31a-47bd4e792345.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 25021-806-01 | 25021080601 | 10 VIAL in 1 CARTON (25021-806-01) > 1 mL in 1 VIAL | 10 vial | 2011-10-24 | 0000-00-00 | No | No | Current |