# LIPFENDRA

NDC: 0006-5084
Generic name: LIPFENDRA
Labeler / Manufacturer: Merck Sharp & Dohme LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260715

FDA application: NDA220848

## Active ingredients

- ENLICITIDE DECANOATE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0006-5084"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0006-5084
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=100ec543-fbd0-44fc-b740-db9cdff39145