lenalidomide

Generic: lenalidomide

Labeler: devatis inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lenalidomide
Generic Name lenalidomide
Labeler devatis inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

lenalidomide 25 mg/1

Manufacturer
Devatis Inc.

Identifiers & Regulatory

Product NDC 73043-043
Product ID 73043-043_0835d82d-196b-4ec8-aa3b-adb7fe501aa2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217554
Listing Expiration 2027-12-31
Marketing Start 2026-01-31

Pharmacologic Class

Established (EPC)
thalidomide analog [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73043043
Hyphenated Format 73043-043

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 ANDA217554 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (73043-043-01)
  • 21 CAPSULE in 1 BOTTLE (73043-043-21)
source: ndc

Packages (2)

Ingredients (1)

lenalidomide (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0835d82d-196b-4ec8-aa3b-adb7fe501aa2", "openfda": {"nui": ["N0000184014"], "unii": ["F0P408N6V4"], "rxcui": ["602910", "602912", "643712", "643720", "1242231", "1428947"], "spl_set_id": ["9959cd7e-12b6-4b59-8205-d5f6e7e7d09b"], "pharm_class_epc": ["Thalidomide Analog [EPC]"], "manufacturer_name": ["Devatis Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (73043-043-01)", "package_ndc": "73043-043-01", "marketing_start_date": "20260131"}, {"sample": false, "description": "21 CAPSULE in 1 BOTTLE (73043-043-21)", "package_ndc": "73043-043-21", "marketing_start_date": "20260131"}], "brand_name": "Lenalidomide", "product_id": "73043-043_0835d82d-196b-4ec8-aa3b-adb7fe501aa2", "dosage_form": "CAPSULE", "pharm_class": ["Thalidomide Analog [EPC]"], "product_ndc": "73043-043", "generic_name": "Lenalidomide", "labeler_name": "Devatis Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lenalidomide", "active_ingredients": [{"name": "LENALIDOMIDE", "strength": "25 mg/1"}], "application_number": "ANDA217554", "marketing_category": "ANDA", "marketing_start_date": "20260131", "listing_expiration_date": "20271231"}