Package 0574-1415-21
Brand: lenalidomide
Generic: lenalidomidePackage Facts
Identity
Package NDC
0574-1415-21
Digits Only
0574141521
Product NDC
0574-1415
Description
21 CAPSULE in 1 BOTTLE (0574-1415-21)
Marketing
Marketing Status
Brand
lenalidomide
Generic
lenalidomide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dffe719b-4f61-47e2-b71c-673322d487f5", "openfda": {"nui": ["N0000184014"], "unii": ["F0P408N6V4"], "rxcui": ["602910", "602912", "643712", "643720", "1242231", "1428947"], "spl_set_id": ["dffe719b-4f61-47e2-b71c-673322d487f5"], "pharm_class_epc": ["Thalidomide Analog [EPC]"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BOTTLE (0574-1415-21)", "package_ndc": "0574-1415-21", "marketing_start_date": "20260131"}], "brand_name": "LENALIDOMIDE", "product_id": "0574-1415_dffe719b-4f61-47e2-b71c-673322d487f5", "dosage_form": "CAPSULE", "pharm_class": ["Thalidomide Analog [EPC]"], "product_ndc": "0574-1415", "generic_name": "lenalidomide", "labeler_name": "Padagis US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LENALIDOMIDE", "active_ingredients": [{"name": "LENALIDOMIDE", "strength": "15 mg/1"}], "application_number": "ANDA217265", "marketing_category": "ANDA", "marketing_start_date": "20260131", "listing_expiration_date": "20261231"}