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Mycophenolate mofetil
Mycophenolate mofetil - 0781-5175-10 - (Mycophenolate mofetil)
Drug Information of Mycophenolate mofetil
| Product NDC: | 0781-5175 |
| Proprietary Name: | Mycophenolate mofetil |
| Non Proprietary Name: | Mycophenolate mofetil |
| Active Ingredient(s): | 500 mg/1 & nbsp; Mycophenolate mofetil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mycophenolate mofetil
| Product NDC: | 0781-5175 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065451 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081015 |
Package Information of Mycophenolate mofetil
| Package NDC: | 0781-5175-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (0781-5175-10) |
NDC Information of Mycophenolate mofetil
| NDC Code | 0781-5175-10 |
| Proprietary Name | Mycophenolate mofetil |
| Package Description | 1000 TABLET in 1 BOTTLE (0781-5175-10) |
| Product NDC | 0781-5175 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mycophenolate mofetil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20081015 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | MYCOPHENOLATE MOFETIL |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimetabolite Immunosuppressant [EPC] |
