NDC 70095-060 – Pomalidomide

Pomalidomide 4 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70095-060

Product details

Brand name
Pomalidomide
Generic name
Pomalidomide
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210232
Marketed since
August 31, 2026
Listing expires
December 31, 2027
Pharmacologic class
Thalidomide Analog

Active ingredients

Uses, dosage, side effects and warnings for Pomalidomide →

Package NDC codes (2)

Package NDCDescriptionSince
70095-060-0121 CAPSULE in 1 BOTTLE (70095-060-01)Aug 31, 2026
70095-060-02100 CAPSULE in 1 BOTTLE (70095-060-02)Aug 31, 2026

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