NDC 71335-9660 – Alprazolam

Alprazolam 1 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-9660

Product details

Brand name
Alprazolam
Generic name
Alprazolam
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203346
Marketed since
July 31, 2015
Listing expires
December 31, 2027
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Alprazolam →

Package NDC codes (10)

Package NDCDescriptionSince
71335-9660-010 TABLET in 1 BOTTLE (71335-9660-0)Oct 24, 2023
71335-9660-128 TABLET in 1 BOTTLE (71335-9660-1)Apr 13, 2026
71335-9660-220 TABLET in 1 BOTTLE (71335-9660-2)May 2, 2023
71335-9660-330 TABLET in 1 BOTTLE (71335-9660-3)Mar 14, 2023
71335-9660-460 TABLET in 1 BOTTLE (71335-9660-4)Mar 29, 2023
71335-9660-590 TABLET in 1 BOTTLE (71335-9660-5)Mar 15, 2023
71335-9660-650 TABLET in 1 BOTTLE (71335-9660-6)Apr 13, 2026
71335-9660-7120 TABLET in 1 BOTTLE (71335-9660-7)Apr 13, 2026
71335-9660-8100 TABLET in 1 BOTTLE (71335-9660-8)Apr 13, 2026
71335-9660-940 TABLET in 1 BOTTLE (71335-9660-9)Apr 13, 2026

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