Details for New Drug Application (NDA): 207474
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The generic ingredient in OXALIPLATIN is oxaliplatin. There is one drug master file entry for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the oxaliplatin profile page.
Summary for 207474
| Tradename: | OXALIPLATIN |
| Applicant: | Accord Hlthcare |
| Ingredient: | oxaliplatin |
| Patents: | 0 |
Suppliers and Packaging for NDA: 207474
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| OXALIPLATIN | oxaliplatin | INJECTABLE;INTRAVENOUS | 207474 | ANDA | Accord Healthcare Inc. | 16729-332 | 16729-332-03 | 1 VIAL, SINGLE-DOSE in 1 CARTON (16729-332-03) / 10 mL in 1 VIAL, SINGLE-DOSE |
| OXALIPLATIN | oxaliplatin | INJECTABLE;INTRAVENOUS | 207474 | ANDA | Accord Healthcare Inc. | 16729-332 | 16729-332-05 | 1 VIAL, SINGLE-DOSE in 1 CARTON (16729-332-05) / 20 mL in 1 VIAL, SINGLE-DOSE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INTRAVENOUS | Strength | 50MG/10ML (5MG/ML) | ||||
| Approval Date: | Mar 21, 2017 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INTRAVENOUS | Strength | 100MG/20ML (5MG/ML) | ||||
| Approval Date: | Mar 21, 2017 | TE: | AP | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INTRAVENOUS | Strength | 200MG/40ML (5MG/ML) | ||||
| Approval Date: | Mar 21, 2017 | TE: | RLD: | No | |||||
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