# HALOPERIDOL

NDC: 72205-067
Generic name: HALOPERIDOL
Labeler / Manufacturer: Novadoz Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20221118

FDA application: ANDA216004

## Active ingredients

- HALOPERIDOL: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72205-067"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72205-067
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3a474e06-fb00-40cb-aa3a-6edad43c2c0a