Haloperidol Decanoate
- Product NDC
- 70518-3097
- 11-digit product format
- 705183097
- Labeler code
- 70518
- Product ID
- 70518-3097_c2a09295-0c57-0b11-e053-2995a90a22a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol Decanoate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075393
- Marketing category
- ANDA
- Marketing start
- 2021-05-18
- 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
- 2022-12-31
- 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 |
|---|
| 70518-3097-0 | 70518309700 | 10 VIAL, SINGLE-DOSE in 1 CARTON (70518-3097-0) > 1 mL in 1 VIAL, SINGLE-DOSE (70518-3097-1) | 2021-05-18 | 0000-00-00 | No | No | Current |