Details for New Drug Application (NDA): 078819
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The generic ingredient in OXALIPLATIN is oxaliplatin. There are twenty-six drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the oxaliplatin profile page.
Summary for 078819
| Tradename: | OXALIPLATIN |
| Applicant: | Fresenius Kabi Usa |
| Ingredient: | oxaliplatin |
| Patents: | 0 |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INTRAVENOUS | Strength | 50MG/VIAL | ||||
| Approval Date: | Jun 2, 2010 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INTRAVENOUS | Strength | 100MG/VIAL | ||||
| Approval Date: | Jun 2, 2010 | TE: | AP | RLD: | No | ||||
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