Package 82293-009-10

Brand: lenalidomide

Generic: lenalidomide
NDC Package

Package Facts

Identity

Package NDC 82293-009-10
Digits Only 8229300910
Product NDC 82293-009
Description

21 CAPSULE in 1 BOTTLE (82293-009-10)

Marketing

Marketing Status
Marketed Since 2026-01-06
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": "4531a3e4-1189-0276-e063-6394a90aedfd", "openfda": {"nui": ["N0000184014"], "upc": ["0382293011100", "0382293008100", "0382293007103"], "unii": ["F0P408N6V4"], "rxcui": ["602910", "602912", "643712", "643720", "1242231", "1428947"], "spl_set_id": ["2166bbdf-eb12-4564-b9e4-b63ca21312bc"], "pharm_class_epc": ["Thalidomide Analog [EPC]"], "manufacturer_name": ["Novugen Pharma (USA) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BOTTLE (82293-009-10)", "package_ndc": "82293-009-10", "marketing_start_date": "20260106"}], "brand_name": "Lenalidomide", "product_id": "82293-009_4531a3e4-1189-0276-e063-6394a90aedfd", "dosage_form": "CAPSULE", "pharm_class": ["Thalidomide Analog [EPC]"], "product_ndc": "82293-009", "generic_name": "Lenalidomide", "labeler_name": "Novugen Pharma (USA) LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lenalidomide", "active_ingredients": [{"name": "LENALIDOMIDE", "strength": "15 mg/1"}], "application_number": "ANDA217281", "marketing_category": "ANDA", "marketing_start_date": "20260106", "listing_expiration_date": "20261231"}