Revlimid - 59572-420-21 - (Lenalidomide)

Alphabetical Index


Drug Information of Revlimid

Product NDC: 59572-420
Proprietary Name: Revlimid
Non Proprietary Name: Lenalidomide
Active Ingredient(s): 20    mg/1 & nbsp;   Lenalidomide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Revlimid

Product NDC: 59572-420
Labeler Name: Celgene Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021880
Marketing Category: NDA
Start Marketing Date: 20130606

Package Information of Revlimid

Package NDC: 59572-420-21
Package Description: 21 CAPSULE in 1 BOTTLE (59572-420-21)

NDC Information of Revlimid

NDC Code 59572-420-21
Proprietary Name Revlimid
Package Description 21 CAPSULE in 1 BOTTLE (59572-420-21)
Product NDC 59572-420
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lenalidomide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130606
Marketing Category Name NDA
Labeler Name Celgene Corporation
Substance Name LENALIDOMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Revlimid


General Information