# LOFEXIDINE

NDC: 85789-901
Generic name: lofexidine hydrochloride
Labeler / Manufacturer: BioCorRx Pharmaceuticals Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260815

FDA application: NDA209229

## Active ingredients

- LOFEXIDINE HYDROCHLORIDE: .2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85789-901"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85789-901
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2dcc8288-adbe-45c3-b7bd-4d274001332d