Anagrelide

NDC 70954-879 · ANI Pharmaceuticals, Inc.

Generic nameAnagrelide

Dosage formCAPSULE

RouteORAL

Active ingredient(s)ANAGRELIDE HYDROCHLORIDE

Strength.5 mg/1

Pharmacologic classDecreased Platelet Production [PE], Phosphodiesterase 3 Inhibitors [MoA], Platelet-reducing Agent [EPC]

Marketing categoryANDA

Packages

70954-879-10 — 100 CAPSULE in 1 BOTTLE (70954-879-10)

FDA lists these products with the same active ingredient.

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