NDC 71335-9667 – Alprazolam

Alprazolam .25 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-9667

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
71335-9667-010 TABLET in 1 BOTTLE (71335-9667-0)Apr 13, 2026
71335-9667-130 TABLET in 1 BOTTLE (71335-9667-1)Mar 13, 2023
71335-9667-2100 TABLET in 1 BOTTLE (71335-9667-2)Apr 13, 2026
71335-9667-360 TABLET in 1 BOTTLE (71335-9667-3)Mar 10, 2023
71335-9667-420 TABLET in 1 BOTTLE (71335-9667-4)Aug 21, 2024
71335-9667-590 TABLET in 1 BOTTLE (71335-9667-5)Mar 30, 2023
71335-9667-615 TABLET in 1 BOTTLE (71335-9667-6)Apr 13, 2026
71335-9667-7120 TABLET in 1 BOTTLE (71335-9667-7)Oct 21, 2024
71335-9667-840 TABLET in 1 BOTTLE (71335-9667-8)Apr 13, 2026
71335-9667-914 TABLET in 1 BOTTLE (71335-9667-9)Apr 16, 2024

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