Package 63304-045-22

Brand: lenalidomide

Generic: lenalidomide
NDC Package

Package Facts

Identity

Package NDC 63304-045-22
Digits Only 6330404522
Product NDC 63304-045
Product ID 63304-045_2922537e-47de-b6b9-e063-6294a90a0f19
Description

21 CAPSULE in 1 BOTTLE (63304-045-22)

Marketing

Marketing Status
Marketed Since 2023-03-12
Brand lenalidomide
Generic lenalidomide
Sample Package No

Linked Drug Pages (1)

Lenalidomide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2922537e-47de-b6b9-e063-6294a90a0f19", "openfda": {"nui": ["N0000184014"], "unii": ["F0P408N6V4"], "rxcui": ["602910", "602912", "643712", "643720", "1242231", "1428947"], "spl_set_id": ["84d9dec7-9250-4dbd-9a0d-23e75f111892"], "pharm_class_epc": ["Thalidomide Analog [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (63304-045-01)", "package_ndc": "63304-045-01", "marketing_start_date": "20230312"}, {"sample": false, "description": "21 CAPSULE in 1 BOTTLE (63304-045-22)", "package_ndc": "63304-045-22", "marketing_start_date": "20230312"}], "brand_name": "Lenalidomide", "product_id": "63304-045_2922537e-47de-b6b9-e063-6294a90a0f19", "dosage_form": "CAPSULE", "pharm_class": ["Thalidomide Analog [EPC]"], "product_ndc": "63304-045", "generic_name": "Lenalidomide", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lenalidomide", "active_ingredients": [{"name": "LENALIDOMIDE", "strength": "20 mg/1"}], "application_number": "ANDA211846", "marketing_category": "ANDA", "marketing_start_date": "20230312", "listing_expiration_date": "20261231"}