# lofexidine hydrochloride

NDC: 72205-246
Generic name: lofexidine hydrochloride
Labeler / Manufacturer: Novadoz Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250224

FDA application: ANDA218699

## 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:"72205-246"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72205-246
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=19b5c932-af2d-4a0b-ac4a-ba06c53c3219