# Bimatoprost

NDC: 62332-507
Generic name: Bimatoprost
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20190412

FDA application: ANDA210263

## Active ingredients

- BIMATOPROST: .3 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-507"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-507
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a4f4ecb2-999f-4656-8f94-2f06c6dd7990