# LEUPROLIDE ACETATE

NDC: 42023-259
Generic name: LEUPROLIDE ACETATE
Labeler / Manufacturer: Endo USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20260630

FDA application: ANDA217437

## Active ingredients

- LEUPROLIDE ACETATE: 1 mg/.2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42023-259"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42023-259
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=290b0716-2fd5-43a1-8d3c-4857c1b2eefa