# LOTEMAX

NDC: 24208-299
Generic name: loteprednol etabonate
Labeler / Manufacturer: Bausch & Lomb Incorporated
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SUSPENSION/ DROPS
Routes: OPHTHALMIC
Marketing started: 19980309

FDA application: NDA020583

## Active ingredients

- LOTEPREDNOL ETABONATE: 5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24208-299"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24208-299
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f37d74ac-5f9c-40a8-b43b-35148fc66bbe