# Lofexidine

NDC: 71921-250
Generic name: Lofexidine
Labeler / Manufacturer: Florida Pharmaceutical Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20240821

FDA application: ANDA218613

## Active ingredients

- LOFEXIDINE HYDROCHLORIDE: .18 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71921-250"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71921-250
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce4488e2-842c-45ba-aca7-075a900e2a1c