Details for New Drug Application (NDA): 211846
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The generic ingredient in LENALIDOMIDE is lenalidomide. There are fourteen drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the lenalidomide profile page.
Summary for 211846
Tradename: | LENALIDOMIDE |
Applicant: | Sun Pharm |
Ingredient: | lenalidomide |
Patents: | 0 |
Suppliers and Packaging for NDA: 211846
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
LENALIDOMIDE | lenalidomide | CAPSULE;ORAL | 211846 | ANDA | Sun Pharmaceutical Industries, Inc. | 63304-041 | 63304-041-01 | 100 CAPSULE in 1 BOTTLE (63304-041-01) |
LENALIDOMIDE | lenalidomide | CAPSULE;ORAL | 211846 | ANDA | Sun Pharmaceutical Industries, Inc. | 63304-041 | 63304-041-27 | 28 CAPSULE in 1 BOTTLE (63304-041-27) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 5MG | ||||
Approval Date: | Feb 8, 2023 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 10MG | ||||
Approval Date: | Feb 8, 2023 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 15MG | ||||
Approval Date: | Feb 8, 2023 | TE: | AB | RLD: | No |
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