# Ofloxacin

NDC: 70069-686
Generic name: Ofloxacin
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: AURICULAR (OTIC)
Marketing started: 20241031

FDA application: ANDA216328

## Active ingredients

- OFLOXACIN: 3 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-686"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-686
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=72ad7b86-1d5b-48c9-bb40-319d6c186f1d
