NDC 0781-2102 – Tacrolimus

Tacrolimus .5 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC0781-2102

Product details

Brand name
Tacrolimus
Generic name
Tacrolimus
Labeler
Sandoz Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA065461
Marketed since
August 10, 2009
Listing expires
December 31, 2027
Pharmacologic class
Calcineurin Inhibitor Immunosuppressant

Active ingredients

Uses, dosage, side effects and warnings for Tacrolimus →

Package NDC codes (1)

Package NDCDescriptionSince
0781-2102-01100 CAPSULE in 1 BOTTLE (0781-2102-01)Aug 10, 2009

Recalls mentioning this NDC

Other Tacrolimus products