# OCUFLOX

NDC: 11980-779
Generic name: ofloxacin
Labeler / Manufacturer: Allergan, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 19930801

FDA application: NDA019921

## 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:"11980-779"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11980-779
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7aab4449-3dda-4e2c-8e40-b3244a548bf5