NDC 62135-313 – Anagrelide

Anagrelide Hydrochloride Anhydrous 1 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC62135-313

Product details

Brand name
Anagrelide
Generic name
Anagrelide
Labeler
Chartwell RX, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA076683
Marketed since
April 18, 2005
Listing expires
December 31, 2026
Pharmacologic class
Platelet-reducing Agent

Active ingredients

Uses, dosage, side effects and warnings for Anagrelide →

Package NDC codes (1)

Package NDCDescriptionSince
62135-313-6060 CAPSULE in 1 BOTTLE (62135-313-60)Feb 5, 2024

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