# LUMIGAN

NDC: 0023-3205
Generic name: bimatoprost
Labeler / Manufacturer: Allergan, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20100910

FDA application: NDA022184

## Active ingredients

- BIMATOPROST: .1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0023-3205"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0023-3205
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a5e67c75-db88-4372-bb07-c8dd15c97631