# TOFACITINIB CITRATE

NDC: 77771-567
Generic name: Tofacitinib citrate
Labeler / Manufacturer: Radha Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260714

FDA application: ANDA220972

## 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:"77771-567"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=77771-567
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=141ab3eb-982b-4242-89db-6ddce5be0c40