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) |
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 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 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] |