Details for New Drug Application (NDA): 215892
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The generic ingredient in CYCLOPHOSPHAMIDE is cyclophosphamide. There are nineteen drug master file entries for this compound. Twenty-four suppliers are listed for this compound. Additional details are available on the cyclophosphamide profile page.
Summary for 215892
| Tradename: | CYCLOPHOSPHAMIDE |
| Applicant: | Alembic |
| Ingredient: | cyclophosphamide |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 215892
Suppliers and Packaging for NDA: 215892
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CYCLOPHOSPHAMIDE | cyclophosphamide | CAPSULE;ORAL | 215892 | ANDA | Alembic Pharmaceuticals Limited | 46708-618 | 46708-618-31 | 100 CAPSULE in 1 BOTTLE (46708-618-31) |
| CYCLOPHOSPHAMIDE | cyclophosphamide | CAPSULE;ORAL | 215892 | ANDA | Alembic Pharmaceuticals Limited | 46708-619 | 46708-619-31 | 100 CAPSULE in 1 BOTTLE (46708-619-31) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 25MG | ||||
| Approval Date: | Nov 10, 2022 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 50MG | ||||
| Approval Date: | Nov 10, 2022 | TE: | AB | RLD: | No | ||||
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