# MOXIFLOXACIN

NDC: 68180-421
Generic name: MOXIFLOXACIN
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20200213

FDA application: ANDA204079

## Active ingredients

- MOXIFLOXACIN HYDROCHLORIDE: 5 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68180-421"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-421
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d66f080b-da56-4473-8785-920d9700f72d