# Simlandi

NDC: 51759-402
Generic name: adalimumab-ryvk
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: KIT
Routes: SUBCUTANEOUS
Marketing started: 20240520

FDA application: BLA761299

## 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:"51759-402"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51759-402
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=12f609c9-2088-bb05-e063-6394a90a9ecc