FDA NDC Directory · JSON-LD · Markdown

Tacrolimus

NDC 0781-2103 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerSandoz Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065461
Dosage form / routeCAPSULE · ORAL
Active ingredientsTACROLIMUS (1 mg/1)
Marketing started20090810
Package count1

External sources

Source: openFDA. Public-domain (CC0).