lenalidomide

Generic: lenalidomide

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lenalidomide
Generic Name lenalidomide
Labeler amneal pharmaceuticals ny llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

lenalidomide 20 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 60219-1718
Product ID 60219-1718_5d131f97-a92e-4266-a3f9-6942be6ec47e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216213
Listing Expiration 2026-12-31
Marketing Start 2025-02-12

Pharmacologic Class

Established (EPC)
thalidomide analog [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 602191718
Hyphenated Format 60219-1718

Supplemental Identifiers

RxCUI
602910 602912 643712 643720 1242231 1428947
UPC
0360219171527
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 ANDA216213 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 21 CAPSULE in 1 BOTTLE (60219-1718-1)
  • 100 CAPSULE in 1 BOTTLE (60219-1718-2)
source: ndc

Packages (2)

Ingredients (1)

lenalidomide (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5d131f97-a92e-4266-a3f9-6942be6ec47e", "openfda": {"nui": ["N0000184014"], "upc": ["0360219171527"], "unii": ["F0P408N6V4"], "rxcui": ["602910", "602912", "643712", "643720", "1242231", "1428947"], "spl_set_id": ["da7b5dda-79ed-4c4a-88aa-52394fdc7c54"], "pharm_class_epc": ["Thalidomide Analog [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BOTTLE (60219-1718-1)", "package_ndc": "60219-1718-1", "marketing_start_date": "20250212"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (60219-1718-2)", "package_ndc": "60219-1718-2", "marketing_start_date": "20250212"}], "brand_name": "LENALIDOMIDE", "product_id": "60219-1718_5d131f97-a92e-4266-a3f9-6942be6ec47e", "dosage_form": "CAPSULE", "pharm_class": ["Thalidomide Analog [EPC]"], "product_ndc": "60219-1718", "generic_name": "lenalidomide", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LENALIDOMIDE", "active_ingredients": [{"name": "LENALIDOMIDE", "strength": "20 mg/1"}], "application_number": "ANDA216213", "marketing_category": "ANDA", "marketing_start_date": "20250212", "listing_expiration_date": "20261231"}