# Tofacitinib

NDC: 42799-970
Generic name: Tofacitinib
Labeler / Manufacturer: Edenbridge Pharmaceuticals LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260603

FDA application: ANDA218668

## Active ingredients

- TOFACITINIB CITRATE: 11 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42799-970"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42799-970
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=576722e5-6639-452d-a5c3-33a064f19481