NDC 52536-341 – Lomustine

Lomustine 40 mg/1 · Capsule, Gelatin Coated · Oral

Human Prescription Drug

Product NDC52536-341

Product details

Brand name
Lomustine
Generic name
Lomustine
Labeler
Wilshire Pharmaceuticals, Inc.
Dosage form
Capsule, Gelatin Coated
Route
Oral
Marketing category
NDA · NDA017588
Marketed since
April 15, 2026
Listing expires
December 31, 2027
Pharmacologic class
Alkylating Drug

Active ingredients

Uses, dosage, side effects and warnings for Lomustine →

Package NDC codes (1)

Package NDCDescriptionSince
52536-341-051 BOTTLE in 1 CARTON (52536-341-05) / 5 CAPSULE, GELATIN COATED in 1 BOTTLEApr 15, 2026

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