Tacrolimus - 0781-2102-01 - (Tacrolimus)

Alphabetical Index


Drug Information of Tacrolimus

Product NDC: 0781-2102
Proprietary Name: Tacrolimus
Non Proprietary Name: Tacrolimus
Active Ingredient(s): .5    mg/1 & nbsp;   Tacrolimus
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Tacrolimus

Product NDC: 0781-2102
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065461
Marketing Category: ANDA
Start Marketing Date: 20090810

Package Information of Tacrolimus

Package NDC: 0781-2102-01
Package Description: 100 CAPSULE in 1 BOTTLE (0781-2102-01)

NDC Information of Tacrolimus

NDC Code 0781-2102-01
Proprietary Name Tacrolimus
Package Description 100 CAPSULE in 1 BOTTLE (0781-2102-01)
Product NDC 0781-2102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tacrolimus
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090810
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name TACROLIMUS
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA]

Complete Information of Tacrolimus


General Information