haloperidol decanoate
- Product NDC
- 70518-1281
- 11-digit product format
- 705181281
- Labeler code
- 70518
- Product ID
- 70518-1281_d92a963d-e1bd-36f3-e053-2995a90ad2ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- haloperidol decanoate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205241
- Marketing category
- ANDA
- Marketing start
- 2018-07-11
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL DECANOATE
- Active strength
- 100 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 |
|---|
| 70518-1281-0 | 70518128100 | 10 VIAL in 1 CARTON (70518-1281-0) > 1 mL in 1 VIAL | 10 vial | 2018-07-11 | 0000-00-00 | No | No | Current |