Tacrolimus - 68084-450-01 - (Tacrolimus)

Alphabetical Index


Drug Information of Tacrolimus

Product NDC: 68084-450
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: 68084-450
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090509
Marketing Category: ANDA
Start Marketing Date: 20100803

Package Information of Tacrolimus

Package NDC: 68084-450-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-450-01) > 10 CAPSULE in 1 BLISTER PACK (68084-450-11)

NDC Information of Tacrolimus

NDC Code 68084-450-01
Proprietary Name Tacrolimus
Package Description 10 BLISTER PACK in 1 CARTON (68084-450-01) > 10 CAPSULE in 1 BLISTER PACK (68084-450-11)
Product NDC 68084-450
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tacrolimus
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100803
Marketing Category Name ANDA
Labeler Name American Health Packaging
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