# HALOPERIDOL

NDC: 82619-107
Generic name: haloperidol
Labeler / Manufacturer: Creekwood Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260105

FDA application: ANDA218162

## Active ingredients

- HALOPERIDOL: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82619-107"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82619-107
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9763c044-7430-48f7-bf3e-da1c7c683955