# Lofexidine

NDC: 70954-909
Generic name: Lofexidine
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20251022

FDA application: ANDA219917

## 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:"70954-909"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-909
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=335e26bf-b236-46d6-81cf-2879e5f3b1d9