Tacrolimus - 50742-208-01 - (tacrolimus)

Alphabetical Index


Drug Information of Tacrolimus

Product NDC: 50742-208
Proprietary Name: Tacrolimus
Non Proprietary Name: tacrolimus
Active Ingredient(s): 1    mg/1 & nbsp;   tacrolimus
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Tacrolimus

Product NDC: 50742-208
Labeler Name: Ingenus Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091195
Marketing Category: ANDA
Start Marketing Date: 20120928

Package Information of Tacrolimus

Package NDC: 50742-208-01
Package Description: 100 CAPSULE in 1 BOTTLE (50742-208-01)

NDC Information of Tacrolimus

NDC Code 50742-208-01
Proprietary Name Tacrolimus
Package Description 100 CAPSULE in 1 BOTTLE (50742-208-01)
Product NDC 50742-208
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tacrolimus
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120928
Marketing Category Name ANDA
Labeler Name Ingenus Pharmaceuticals, LLC
Substance Name TACROLIMUS
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA]

Complete Information of Tacrolimus


General Information