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mycophenolate mofetil
mycophenolate mofetil - 59762-0702-1 - (mycophenolate mofetil)
Drug Information of mycophenolate mofetil
| Product NDC: | 59762-0702 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of mycophenolate mofetil
| Product NDC: | 59762-0702 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090456 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100611 |
Package Information of mycophenolate mofetil
| Package NDC: | 59762-0702-1 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59762-0702-1) |
NDC Information of mycophenolate mofetil
| NDC Code | 59762-0702-1 |
| Proprietary Name | mycophenolate mofetil |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59762-0702-1) |
| Product NDC | 59762-0702 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | mycophenolate mofetil |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100611 |
| Marketing Category Name | ANDA |
| Labeler Name | Greenstone LLC |
| Substance Name | MYCOPHENOLATE MOFETIL |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimetabolite Immunosuppressant [EPC] |
