Tacrolimus - 51079-817-20 - (Tacrolimus)

Alphabetical Index


Drug Information of Tacrolimus

Product NDC: 51079-817
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: 51079-817
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090596
Marketing Category: ANDA
Start Marketing Date: 20101104

Package Information of Tacrolimus

Package NDC: 51079-817-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-817-20) > 1 CAPSULE in 1 BLISTER PACK (51079-817-01)

NDC Information of Tacrolimus

NDC Code 51079-817-20
Proprietary Name Tacrolimus
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-817-20) > 1 CAPSULE in 1 BLISTER PACK (51079-817-01)
Product NDC 51079-817
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tacrolimus
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101104
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name TACROLIMUS
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Tacrolimus


General Information