Tacrolimus - 62175-380-37 - (Tacrolimus)

Alphabetical Index


Drug Information of Tacrolimus

Product NDC: 62175-380
Proprietary Name: Tacrolimus
Non Proprietary Name: Tacrolimus
Active Ingredient(s): .5    mg/1 & nbsp;   Tacrolimus
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tacrolimus

Product NDC: 62175-380
Labeler Name: Kremers Urban Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090802
Marketing Category: ANDA
Start Marketing Date: 20121030

Package Information of Tacrolimus

Package NDC: 62175-380-37
Package Description: 100 CAPSULE, GELATIN COATED in 1 BOTTLE (62175-380-37)

NDC Information of Tacrolimus

NDC Code 62175-380-37
Proprietary Name Tacrolimus
Package Description 100 CAPSULE, GELATIN COATED in 1 BOTTLE (62175-380-37)
Product NDC 62175-380
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tacrolimus
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20121030
Marketing Category Name ANDA
Labeler Name Kremers Urban Pharmaceuticals 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