# tacrolimus

NDC: 71432-2002
Generic name: tacrolimus extended-release capsules
Labeler / Manufacturer: Chengdu Suncadia Medicine Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20240125

FDA application: ANDA215012

## Active ingredients

- TACROLIMUS: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71432-2002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71432-2002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=08cf2861-2483-405d-a872-a88a5c235f9a