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Tacrolimus

NDC 69238-2780 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215012
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsTACROLIMUS (.5 mg/1)
Marketing started20260302
Package count1

External sources

Source: openFDA. Public-domain (CC0).