NDC 70771-1680 – Lenalidomide

Lenalidomide 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70771-1680

Product details

Brand name
Lenalidomide
Generic name
Lenalidomide
Labeler
Zydus Lifesciences Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210154
Marketed since
March 7, 2023
Listing expires
December 31, 2026
Pharmacologic class
Thalidomide Analog

Active ingredients

Uses, dosage, side effects and warnings for Lenalidomide →

Package NDC codes (2)

Package NDCDescriptionSince
70771-1680-1100 CAPSULE in 1 BOTTLE (70771-1680-1)Mar 7, 2023
70771-1680-821 CAPSULE in 1 BOTTLE (70771-1680-8)Mar 7, 2023

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