# leuprolide acetate

NDC: 47335-936
Generic name: leuprolide acetate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: —
Marketing started: 20141215

FDA application: ANDA078885

## 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:"47335-936"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-936
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a3b01473-30c7-4945-bd60-2484221aaaad