# Tacrolimus

NDC: 0781-2103
Generic name: Tacrolimus
Labeler / Manufacturer: Sandoz Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20090810

FDA application: ANDA065461

## 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:"0781-2103"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-2103
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=46ac55cf-d85e-4c34-bb33-f49e078c4a03