lenalidomide
Generic: lenalidomide
Labeler: exelan pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
lenalidomide
Generic Name
lenalidomide
Labeler
exelan pharmaceuticals inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
lenalidomide 2.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
76282-696
Product ID
76282-696_ecb5abfb-3a17-4235-a7fe-0183c5586738
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214618
Listing Expiration
2026-12-31
Marketing Start
2024-06-10
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76282696
Hyphenated Format
76282-696
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
lenalidomide (source: ndc)
Generic Name
lenalidomide (source: ndc)
Application Number
ANDA214618 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.5 mg/1
Packaging
- 28 CAPSULE in 1 BOTTLE (76282-696-48)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ecb5abfb-3a17-4235-a7fe-0183c5586738", "openfda": {"nui": ["N0000184014"], "unii": ["F0P408N6V4"], "rxcui": ["1242231"], "spl_set_id": ["85f5db5d-8f76-46f6-b975-6acda8c4b2c8"], "pharm_class_epc": ["Thalidomide Analog [EPC]"], "manufacturer_name": ["EXELAN PHARMACEUTICALS INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "28 CAPSULE in 1 BOTTLE (76282-696-48)", "package_ndc": "76282-696-48", "marketing_start_date": "20240610"}], "brand_name": "LENALIDOMIDE", "product_id": "76282-696_ecb5abfb-3a17-4235-a7fe-0183c5586738", "dosage_form": "CAPSULE", "pharm_class": ["Thalidomide Analog [EPC]"], "product_ndc": "76282-696", "generic_name": "LENALIDOMIDE", "labeler_name": "EXELAN PHARMACEUTICALS INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LENALIDOMIDE", "active_ingredients": [{"name": "LENALIDOMIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA214618", "marketing_category": "ANDA", "marketing_start_date": "20240610", "listing_expiration_date": "20261231"}