# Haloperidol

NDC: 54838-501
Generic name: Haloperidol
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 19930928

FDA application: ANDA073364

## Active ingredients

- HALOPERIDOL LACTATE: 2 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"54838-501"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54838-501
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e44fed0-6132-4881-a9cd-af6156c7af9c