NDC 0093-8199 – Sunitinib Malate

Sunitinib Malate 12.5 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC0093-8199

Product details

Brand name
Sunitinib Malate
Generic name
Sunitinib Malate
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA213803
Marketed since
December 22, 2021
Listing expires
December 31, 2027
Pharmacologic class
Kinase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sunitinib Malate →

Package NDC codes (1)

Package NDCDescriptionSince
0093-8199-2828 CAPSULE in 1 BOTTLE (0093-8199-28)Dec 22, 2021

Recalls mentioning this NDC

Other Sunitinib Malate products