Tacrolimus

NDC 69238-2781 · Amneal Pharmaceuticals NY LLC

Generic nameTacrolimus

Dosage formCAPSULE, EXTENDED RELEASE

RouteORAL

Active ingredient(s)TACROLIMUS

Strength1 mg/1

Pharmacologic classCalcineurin Inhibitor Immunosuppressant [EPC], Calcineurin Inhibitors [MoA]

Marketing categoryANDA

Packages

69238-2781-3 — 1 BAG in 1 CARTON (69238-2781-3) / 3 BLISTER PACK in 1 BAG / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

68254-5006 — Tacrolimus, 68462-534 — Tacrolimus, 68462-685 — tacrolimus, 68462-686 — tacrolimus, 68462-687 — tacrolimus, 68462-881 — Tacrolimus, 68992-3010 — Tacrolimus, 68992-3040 — Tacrolimus, 68992-3075 — Tacrolimus, 69238-2780 — Tacrolimus, 69238-2782 — Tacrolimus, 70377-014 — Tacrolimus, 70377-015 — Tacrolimus, 70377-016 — Tacrolimus, 71335-2189 — Tacrolimus, 71432-2001 — tacrolimus extended-release capsules, 71432-2002 — tacrolimus extended-release capsules, 71432-2003 — tacrolimus extended-release capsules, 72189-536 — Tacrolimus, 82009-054 — Tacrolimus, +83 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.