# Haloperidol

NDC: 76045-737
Generic name: haloperidol lactate
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 20190701

FDA application: ANDA210356

## Active ingredients

- HALOPERIDOL LACTATE: 5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76045-737"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76045-737
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a9970612-0ab3-4a8b-ae84-231738d913a4