# Moxifloxacin

NDC: 33342-322
Generic name: Moxifloxacin
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260302

FDA application: ANDA209143

## Active ingredients

- MOXIFLOXACIN HYDROCHLORIDE: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-322"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-322
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=182ecd0f-714f-42f0-9b16-fb604cf15786