# Tacrolimus

NDC: 69238-2782
Generic name: Tacrolimus
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260302

FDA application: ANDA215012

## Active ingredients

- TACROLIMUS: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69238-2782"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69238-2782
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4eb1b6bd-beec-4dd5-9a48-c93a9fe918b3