HALOPERIDOL LACTATE
- Product NDC
- 70518-1053
- 11-digit product format
- 705181053
- Labeler code
- 70518
- Product ID
- 70518-1053_e5572f3a-47c8-3073-e053-2995a90a5ff8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HALOPERIDOL LACTATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078347
- Marketing category
- ANDA
- Marketing start
- 2018-03-07
- 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 |
|---|
| 70518-1053-0 | 70518105300 | 25 VIAL in 1 CARTON (70518-1053-0) > 1 mL in 1 VIAL (70518-1053-1) | 25 vial | 2018-03-07 | 0000-00-00 | No | No | Current |