# leuprolide acetate

NDC: 70121-2537
Generic name: leuprolide acetate
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: SUBCUTANEOUS
Marketing started: 20221107

FDA application: ANDA215336

## 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:"70121-2537"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70121-2537
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4838c674-044e-46b2-81e7-c691b99d8fa5