NDC 73043-042 – Lenalidomide

Lenalidomide 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC73043-042

Product details

Brand name
Lenalidomide
Generic name
Lenalidomide
Labeler
Devatis Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA217554
Marketed since
January 31, 2026
Listing expires
December 31, 2027
Pharmacologic class
Thalidomide Analog

Active ingredients

Uses, dosage, side effects and warnings for Lenalidomide →

Package NDC codes (2)

Package NDCDescriptionSince
73043-042-01100 CAPSULE in 1 BOTTLE (73043-042-01)Jan 31, 2026
73043-042-2121 CAPSULE in 1 BOTTLE (73043-042-21)Jan 31, 2026

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