lenalidomide
Generic: lenalidomide
Labeler: dr. reddy's laboratories inc.Drug Facts
Product Profile
Brand Name
lenalidomide
Generic Name
lenalidomide
Labeler
dr. reddy's laboratories inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
lenalidomide 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43598-512
Product ID
43598-512_023f2dc9-b878-9d13-44d0-894310c6b8da
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209348
Listing Expiration
2026-12-31
Marketing Start
2022-09-07
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43598512
Hyphenated Format
43598-512
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
ANDA209348 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (43598-512-01)
- 28 CAPSULE in 1 BOTTLE (43598-512-63)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "023f2dc9-b878-9d13-44d0-894310c6b8da", "openfda": {"nui": ["N0000184014"], "unii": ["F0P408N6V4"], "rxcui": ["602910", "602912", "643712", "643720", "1242231", "1428947"], "spl_set_id": ["ca8cc2cc-c856-e676-4f60-1e46d7b53d73"], "pharm_class_epc": ["Thalidomide Analog [EPC]"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (43598-512-01)", "package_ndc": "43598-512-01", "marketing_start_date": "20220907"}, {"sample": false, "description": "28 CAPSULE in 1 BOTTLE (43598-512-63)", "package_ndc": "43598-512-63", "marketing_start_date": "20220907"}], "brand_name": "Lenalidomide", "product_id": "43598-512_023f2dc9-b878-9d13-44d0-894310c6b8da", "dosage_form": "CAPSULE", "pharm_class": ["Thalidomide Analog [EPC]"], "product_ndc": "43598-512", "generic_name": "Lenalidomide", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lenalidomide", "active_ingredients": [{"name": "LENALIDOMIDE", "strength": "10 mg/1"}], "application_number": "ANDA209348", "marketing_category": "ANDA", "marketing_start_date": "20220907", "listing_expiration_date": "20261231"}