NDC 24338-340 – Gleostine

Lomustine 10 mg/1 · Capsule, Gelatin Coated · Oral

Human Prescription Drug

Product NDC24338-340

Product details

Brand name
Gleostine
Generic name
lomustine
Labeler
Azurity Pharmaceuticals, Inc.
Dosage form
Capsule, Gelatin Coated
Route
Oral
Marketing category
NDA · NDA017588
Marketed since
October 24, 2025
Listing expires
December 31, 2026
Pharmacologic class
Alkylating Drug

Active ingredients

Uses, dosage, side effects and warnings for Gleostine →

Package NDC codes (1)

Package NDCDescriptionSince
24338-340-051 BOTTLE in 1 CARTON (24338-340-05) / 5 CAPSULE, GELATIN COATED in 1 BOTTLEOct 24, 2025

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