# Moxifloxacin

NDC: 68180-422
Generic name: Moxifloxacin
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20170701

FDA application: ANDA202867

## 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:"68180-422"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-422
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ae77e219-8af9-4aa4-96d3-05c9726a1d3c