NDC 59762-3721 – Alprazolam

Alprazolam 1 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV 1 recall

Product NDC59762-3721

Product details

Brand name
Alprazolam
Generic name
alprazolam
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA018276
Marketed since
October 16, 1981
Listing expires
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Alprazolam →

Package NDC codes (3)

Package NDCDescriptionSince
59762-3721-1100 TABLET in 1 BOTTLE (59762-3721-1)Oct 16, 1981
59762-3721-3500 TABLET in 1 BOTTLE (59762-3721-3)Oct 16, 1981
59762-3721-41000 TABLET in 1 BOTTLE (59762-3721-4)Oct 16, 1981

Recalls mentioning this NDC

Other Alprazolam products