# BROMSITE 0.075%

NDC: 49708-754
Generic name: bromfenac
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20160501

FDA application: NDA206911

## Active ingredients

- BROMFENAC SODIUM: .76 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"49708-754"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49708-754
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=144a5072-341b-4591-8705-773b63044bcc