# Everolimus

NDC: 51991-822
Generic name: Everolimus
Labeler / Manufacturer: Breckenridge Pharmaceutical, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210305

FDA application: ANDA205426

## Active ingredients

- EVEROLIMUS: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51991-822"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51991-822
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=01f7b5fb-be0d-4adf-acd2-6899018de966