NDC 0009-0090 – Xanax

Alprazolam 1 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV 1 recall

Product NDC0009-0090

Product details

Brand name
Xanax
Generic name
Alprazolam
Labeler
PHARMACIA & UPJOHN COMPANY LLC
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA018276
Marketed since
October 16, 1981
Marketing end
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Xanax →

Package NDC codes (1)

Package NDCDescriptionSince
0009-0090-04500 TABLET in 1 BOTTLE (0009-0090-04)Oct 16, 1981

Recalls mentioning this NDC

Other Xanax products