# Bimatoprost

NDC: 68071-3590
Generic name: Bimatoprost
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20200810

FDA application: ANDA210126

## Active ingredients

- BIMATOPROST: .3 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-3590"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3590
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=147e2ec6-8fb1-ed5a-e063-6294a90a5eca