Product NDC: | 55154-6262 |
Proprietary Name: | Mycophenolate Mofetil |
Non Proprietary Name: | mycophenolate mofetil |
Active Ingredient(s): | 250 mg/1 & nbsp; mycophenolate mofetil |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-6262 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065520 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111025 |
Package NDC: | 55154-6262-0 |
Package Description: | 10 BLISTER PACK in 1 BAG (55154-6262-0) > 1 CAPSULE in 1 BLISTER PACK |
NDC Code | 55154-6262-0 |
Proprietary Name | Mycophenolate Mofetil |
Package Description | 10 BLISTER PACK in 1 BAG (55154-6262-0) > 1 CAPSULE in 1 BLISTER PACK |
Product NDC | 55154-6262 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | mycophenolate mofetil |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20111025 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | MYCOPHENOLATE MOFETIL |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Antimetabolite Immunosuppressant [EPC] |