NDC 71335-2133 – Alprazolam

Alprazolam .25 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-2133

Product details

Brand name
Alprazolam
Generic name
Alprazolam
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074342
Marketed since
October 1, 1993
Listing expires
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Alprazolam →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2133-010 TABLET in 1 BOTTLE (71335-2133-0)Jul 27, 2022
71335-2133-130 TABLET in 1 BOTTLE (71335-2133-1)Jul 27, 2022
71335-2133-2100 TABLET in 1 BOTTLE (71335-2133-2)Jul 27, 2022
71335-2133-360 TABLET in 1 BOTTLE (71335-2133-3)Jul 27, 2022
71335-2133-420 TABLET in 1 BOTTLE (71335-2133-4)Jul 27, 2022
71335-2133-590 TABLET in 1 BOTTLE (71335-2133-5)Jul 27, 2022
71335-2133-615 TABLET in 1 BOTTLE (71335-2133-6)Jul 27, 2022
71335-2133-7120 TABLET in 1 BOTTLE (71335-2133-7)Jul 27, 2022
71335-2133-840 TABLET in 1 BOTTLE (71335-2133-8)Jul 27, 2022
71335-2133-914 TABLET in 1 BOTTLE (71335-2133-9)Jul 27, 2022

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