HALOPERIDOL DECANOATE
- Product NDC
- 70518-2520
- 11-digit product format
- 705182520
- Labeler code
- 70518
- Product ID
- 70518-2520_dc144520-faf1-8c48-e053-2995a90acbe0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HALOPERIDOL DECANOATE
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209101
- Marketing category
- ANDA
- Marketing start
- 2020-01-02
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL DECANOATE
- Active strength
- 50 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 |
|---|
| 70518-2520-0 | 70518252000 | 10 VIAL, SINGLE-DOSE in 1 CARTON (70518-2520-0) > 1 mL in 1 VIAL, SINGLE-DOSE (70518-2520-1) | 2020-01-02 | 0000-00-00 | No | No | Current |