Package 0480-1246-21

Brand: lenalidomide

Generic: lenalidomide
NDC Package

Package Facts

Identity

Package NDC 0480-1246-21
Digits Only 0480124621
Product NDC 0480-1246
Description

21 CAPSULE in 1 BOTTLE (0480-1246-21)

Marketing

Marketing Status
Marketed Since 2022-03-03
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": "f264d32e-0ed0-49b6-80f7-8009ee4803ca", "openfda": {"nui": ["N0000184014"], "upc": ["0304801242288", "0304801246217", "0304801244213", "0304801243285"], "unii": ["F0P408N6V4"], "rxcui": ["602910", "602912", "643712", "643720", "1242231", "1428947"], "spl_set_id": ["1b2716cf-24b4-4157-a218-58ede63917bd"], "pharm_class_epc": ["Thalidomide Analog [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BOTTLE (0480-1246-21)", "package_ndc": "0480-1246-21", "marketing_start_date": "20220303"}], "brand_name": "Lenalidomide", "product_id": "0480-1246_f264d32e-0ed0-49b6-80f7-8009ee4803ca", "dosage_form": "CAPSULE", "pharm_class": ["Thalidomide Analog [EPC]"], "product_ndc": "0480-1246", "generic_name": "Lenalidomide", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lenalidomide", "active_ingredients": [{"name": "LENALIDOMIDE", "strength": "25 mg/1"}], "application_number": "ANDA201452", "marketing_category": "ANDA", "marketing_start_date": "20220303", "listing_expiration_date": "20271231"}