Pomalidomide

NDC 51991-342 · Breckenridge Pharmaceutical, Inc.

Generic namePomalidomide

Dosage formCAPSULE

RouteORAL

Active ingredient(s)POMALIDOMIDE

Strength1 mg/1

Pharmacologic classThalidomide Analog [EPC]

Marketing categoryANDA

Packages

51991-342-21 — 21 CAPSULE in 1 BOTTLE, PLASTIC (51991-342-21)

FDA lists these products with the same active ingredient.

0480-2601 — Pomalidomide, 0480-4018 — Pomalidomide, 0480-4022 — Pomalidomide, 0480-4035 — Pomalidomide, 31722-770 — Pomalidomide, 31722-771 — Pomalidomide, 31722-772 — Pomalidomide, 31722-773 — Pomalidomide, 51991-343 — Pomalidomide, 51991-344 — Pomalidomide, 51991-346 — Pomalidomide, 59572-501 — pomalidomide, 59572-502 — pomalidomide, 59572-503 — pomalidomide, 59572-504 — pomalidomide, 59651-194 — Pomalidomide, 59651-195 — Pomalidomide, 59651-196 — Pomalidomide, 59651-197 — Pomalidomide, 60505-4497 — Pomalidomide, +7 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.