# leuprolide acetate

NDC: 72843-591
Generic name: leuprolide acetate
Labeler / Manufacturer: UBI Pharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: SUBCUTANEOUS
Marketing started: 20241025

FDA application: ANDA217957

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72843-591"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72843-591
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cd46628f-055f-4da9-8c38-fa69af34eb4d