NDC 67877-538 – Temozolomide

Temozolomide 20 mg/1 · Capsule · Oral

Human Prescription Drug 6 recalls

Product NDC67877-538

Product details

Brand name
Temozolomide
Generic name
Temozolomide
Labeler
Ascend Laboratories, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA207658
Marketed since
April 28, 2017
Listing expires
December 31, 2026
Pharmacologic class
Alkylating Drug

Active ingredients

Uses, dosage, side effects and warnings for Temozolomide →

Package NDC codes (2)

Package NDCDescriptionSince
67877-538-075 CAPSULE in 1 BOTTLE (67877-538-07)Apr 28, 2017
67877-538-1414 CAPSULE in 1 BOTTLE (67877-538-14)Apr 28, 2017

Recalls mentioning this NDC

Other Temozolomide products