NDC 16571-821 – Temozolomide

Temozolomide 250 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC16571-821

Product details

Brand name
Temozolomide
Generic name
Temozolomide
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA206309
Marketed since
October 4, 2022
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
16571-821-0220 CAPSULE in 1 BOTTLE (16571-821-02)Oct 4, 2022
16571-821-515 CAPSULE in 1 BOTTLE (16571-821-51)Oct 4, 2022

Recalls mentioning this NDC

Other Temozolomide products