# Haloperidol

NDC: 70518-0035
Generic name: HALOPERIDOL LACTATE
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 20161202

FDA application: ANDA075689

## 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:"70518-0035"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-0035
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e702b2f0-d464-41c3-977a-d37bb22c0ab0