# TOFACITINIB

NDC: 70095-008
Generic name: Tofacitinib
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20260603

FDA application: ANDA218407

## Active ingredients

- TOFACITINIB CITRATE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70095-008"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70095-008
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a764a133-b870-4514-bbee-24d43f8cb7fd