Tacrolimus - 16729-042-01 - (Tacrolimus)

Alphabetical Index


Drug Information of Tacrolimus

Product NDC: 16729-042
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: 16729-042
Labeler Name: Accord Heathcare, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091195
Marketing Category: ANDA
Start Marketing Date: 20110615

Package Information of Tacrolimus

Package NDC: 16729-042-01
Package Description: 100 CAPSULE in 1 BOTTLE (16729-042-01)

NDC Information of Tacrolimus

NDC Code 16729-042-01
Proprietary Name Tacrolimus
Package Description 100 CAPSULE in 1 BOTTLE (16729-042-01)
Product NDC 16729-042
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tacrolimus
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110615
Marketing Category Name ANDA
Labeler Name Accord Heathcare, Inc.
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