Details for New Drug Application (NDA): 065110
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NDA 065110 describes CYCLOSPORINE, which is a drug marketed by Apotex, Dr Reddys Labs Sa, Ivax Sub Teva Pharms, Sandoz, Strides Pharma, Mylan, Teva Pharms Usa Inc, Hikma, Padagis Us, Abbvie, Pharm Assoc, and Pharmobedient Cnsltg, and is included in sixteen NDAs. It is available from ten suppliers. Additional details are available on the CYCLOSPORINE profile page.
The generic ingredient in CYCLOSPORINE is cyclosporine. There are eighteen drug master file entries for this compound. Eighteen suppliers are listed for this compound. Additional details are available on the cyclosporine profile page.
The generic ingredient in CYCLOSPORINE is cyclosporine. There are eighteen drug master file entries for this compound. Eighteen suppliers are listed for this compound. Additional details are available on the cyclosporine profile page.
Summary for 065110
| Tradename: | CYCLOSPORINE |
| Applicant: | Ivax Sub Teva Pharms |
| Ingredient: | cyclosporine |
| Patents: | 0 |
| Formulation / Manufacturing: | see details |
Pharmacology for NDA: 065110
| Mechanism of Action | Calcineurin Inhibitors Cytochrome P450 3A4 Inhibitors P-Glycoprotein Inhibitors |
Medical Subject Heading (MeSH) Categories for 065110
Suppliers and Packaging for NDA: 065110
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CYCLOSPORINE | cyclosporine | CAPSULE;ORAL | 065110 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-9018 | 0093-9018-65 | 30 BLISTER PACK in 1 CARTON (0093-9018-65) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0093-9018-19) |
| CYCLOSPORINE | cyclosporine | CAPSULE;ORAL | 065110 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-9019 | 0093-9019-65 | 30 BLISTER PACK in 1 CARTON (0093-9019-65) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0093-9019-19) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 50MG | ||||
| Approval Date: | Mar 29, 2005 | TE: | AB1 | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 100MG | ||||
| Approval Date: | Mar 29, 2005 | TE: | AB1 | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 25MG | ||||
| Approval Date: | Mar 29, 2005 | TE: | AB1 | RLD: | No | ||||
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