Home
>
National Drug Code (NDC)
>
CellCept
CellCept - 21695-171-00 - (Mycophenolate Mofetil)
Drug Information of CellCept
| Product NDC: | 21695-171 |
| Proprietary Name: | CellCept |
| 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) |
Labeler Information of CellCept
| Product NDC: | 21695-171 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050722 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19950503 |
Package Information of CellCept
| Package NDC: | 21695-171-00 |
| Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (21695-171-00) |
NDC Information of CellCept
| NDC Code | 21695-171-00 |
| Proprietary Name | CellCept |
| Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (21695-171-00) |
| Product NDC | 21695-171 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mycophenolate Mofetil |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19950503 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | MYCOPHENOLATE MOFETIL |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimetabolite Immunosuppressant [EPC] |
