Haloperidol
- Product NDC
- 70518-0776
- 11-digit product format
- 705180776
- Labeler code
- 70518
- Product ID
- 70518-0776_d88d5ece-adb4-3c41-e053-2a95a90a8105
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol lactate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075858
- Marketing category
- ANDA
- Marketing start
- 2019-04-15
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0776-1 | 70518077601 | 25 VIAL in 1 BOX (70518-0776-1) > 1 mL in 1 VIAL (70518-0776-0) | 25 vial | 2019-04-15 | 0000-00-00 | No | No | Current |