# Moxifloxacin Hydrochloride Tablets, 400 mg

NDC: 72205-001
Generic name: Moxifloxacin Hydrochloride Tablets, 400 mg
Labeler / Manufacturer: Novadoz Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180721

FDA application: ANDA208682

## Active ingredients

- MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72205-001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72205-001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=04e0936f-2248-48e4-8031-ac6ccc2df294