Tacrolimus

Product NDC
0781-9303
11-digit product format
007819303
Labeler code
0781
Product ID
0781-9303_9d5be1ff-0d4e-47a8-92f4-6a359e623045
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tacrolimus
Dosage form
CAPSULE
Route
ORAL
Labeler
Sandoz Inc
Application
ANDA065461
Marketing category
ANDA
Marketing start
2012-01-15
Marketing end
0000-00-00
Substance
TACROLIMUS
Active strength
1 mg/1
Pharmacologic classes
Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-9303-01EA - Each0781-9303add7d9f1-ecf9-467a-ab36-d59ccf820d5912012-07-24