Haloperidol
- Product NDC
- 17478-110
- 11-digit product format
- 174780110
- Labeler code
- 17478
- Product ID
- 17478-110_562e5184-a0b4-48c3-97f2-b30587aadbfa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol Lactate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- Akorn
- Application
- ANDA204849
- Marketing category
- ANDA
- Marketing start
- 2017-09-06
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-110-01 | 17478011001 | 10 VIAL, SINGLE-DOSE in 1 CARTON (17478-110-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2017-09-06 | 0000-00-00 | No | No | Current |