NDC 58151-506 – Xanax XR

Alprazolam 3 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CIV 1 recall

Product NDC58151-506

Product details

Brand name
Xanax XR
Generic name
alprazolam
Labeler
Viatris Specialty LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
NDA · NDA021434
Marketed since
July 26, 2024
Marketing end
February 28, 2027
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Xanax →

Package NDC codes (1)

Package NDCDescriptionSince
58151-506-9160 TABLET, EXTENDED RELEASE in 1 BOTTLE (58151-506-91)Jul 26, 2024

Recalls mentioning this NDC

Other Xanax products