# Moxifloxacin

NDC: 80425-0239
Generic name: Moxifloxacin
Labeler / Manufacturer: Advanced Rx Pharmacy of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20230111

FDA application: ANDA090080

## Active ingredients

- MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE: 5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0239"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0239
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f19fa89e-9f5d-4eed-e053-2995a90ac3ce