Thalomid - 59572-205-94 - (Thalidomide)

Alphabetical Index


Drug Information of Thalomid

Product NDC: 59572-205
Proprietary Name: Thalomid
Non Proprietary Name: Thalidomide
Active Ingredient(s): 50    mg/1 & nbsp;   Thalidomide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Thalomid

Product NDC: 59572-205
Labeler Name: Celgene Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020785
Marketing Category: NDA
Start Marketing Date: 20030620

Package Information of Thalomid

Package NDC: 59572-205-94
Package Description: 10 BLISTER PACK in 1 BOX (59572-205-94) > 28 CAPSULE in 1 BLISTER PACK (59572-205-14)

NDC Information of Thalomid

NDC Code 59572-205-94
Proprietary Name Thalomid
Package Description 10 BLISTER PACK in 1 BOX (59572-205-94) > 28 CAPSULE in 1 BLISTER PACK (59572-205-14)
Product NDC 59572-205
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Thalidomide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20030620
Marketing Category Name NDA
Labeler Name Celgene Corporation
Substance Name THALIDOMIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Decreased Immunologically Active Molecule Activity [PE]

Complete Information of Thalomid


General Information