lenalidomide

Generic: lenalidomide

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lenalidomide
Generic Name lenalidomide
Labeler aurobindo pharma limited
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

lenalidomide 10 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-344
Product ID 59651-344_f022fe20-76ac-4825-8986-6e1ec95b0b21
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213885
Listing Expiration 2026-12-31
Marketing Start 2023-03-06

Pharmacologic Class

Established (EPC)
thalidomide analog [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651344
Hyphenated Format 59651-344

Supplemental Identifiers

RxCUI
602910 602912 643712 643720 1242231 1428947
UNII
F0P408N6V4
NUI
N0000184014

Packaging Origin

Original Packager
true

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 ANDA213885 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (59651-344-01)
  • 1 BLISTER PACK in 1 CARTON (59651-344-07) / 7 CAPSULE in 1 BLISTER PACK
  • 28 CAPSULE in 1 BOTTLE (59651-344-28)
source: ndc

Packages (3)

Ingredients (1)

lenalidomide (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f022fe20-76ac-4825-8986-6e1ec95b0b21", "openfda": {"nui": ["N0000184014"], "unii": ["F0P408N6V4"], "rxcui": ["602910", "602912", "643712", "643720", "1242231", "1428947"], "spl_set_id": ["51bfdd53-8fd9-4f86-bebe-75de29e6379d"], "pharm_class_epc": ["Thalidomide Analog [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (59651-344-01)", "package_ndc": "59651-344-01", "marketing_start_date": "20230306"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (59651-344-07)  / 7 CAPSULE in 1 BLISTER PACK", "package_ndc": "59651-344-07", "marketing_start_date": "20230306"}, {"sample": false, "description": "28 CAPSULE in 1 BOTTLE (59651-344-28)", "package_ndc": "59651-344-28", "marketing_start_date": "20230306"}], "brand_name": "Lenalidomide", "product_id": "59651-344_f022fe20-76ac-4825-8986-6e1ec95b0b21", "dosage_form": "CAPSULE", "pharm_class": ["Thalidomide Analog [EPC]"], "product_ndc": "59651-344", "generic_name": "Lenalidomide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lenalidomide", "active_ingredients": [{"name": "LENALIDOMIDE", "strength": "10 mg/1"}], "application_number": "ANDA213885", "marketing_category": "ANDA", "marketing_start_date": "20230306", "listing_expiration_date": "20261231"}