# CAMCEVI

NDC: 69448-023
Generic name: LEUPROLIDE
Labeler / Manufacturer: Accord BioPharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, EMULSION
Routes: SUBCUTANEOUS
Marketing started: 20250519

FDA application: NDA211488

## Active ingredients

- LEUPROLIDE MESYLATE: 42 mg/.37g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69448-023"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69448-023
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cbff25e5-6fe8-4e44-b10a-8397b3349905