Haloperidol
- Product NDC
- 76045-737
- 11-digit product format
- 760450737
- Labeler code
- 76045
- Product ID
- 76045-737_740165fb-1e22-44ae-bc3e-3b66a6862c1a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- haloperidol lactate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- Fresenius Kabi USA, LLC
- Application
- ANDA210356
- Marketing category
- ANDA
- Marketing start
- 2019-07-01
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76045-737 | HALOPERIDOL (HALOPERIDOL LACTATE) INJECTION, SOLUTION [FRESENIUS KABI USA, LLC
] | 18 | Legacy NDC | 20211212_a9970612-0ab3-4a8b-ae84-231738d913a4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76045-737-10 | 76045073710 | 24 SYRINGE in 1 CARTON (76045-737-10) > 1 mL in 1 SYRINGE (76045-737-01) | 24 syringe | 2019-07-01 | 0000-00-00 | No | No | Current |