# Leuprolide Acetate

NDC: 0781-4003
Generic name: Leuprolide Acetate
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: —
Marketing started: 19980804

FDA application: ANDA074728

## 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:"0781-4003"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-4003
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8bd72c1e-2751-4498-a346-bc5e3acbba0b