NDC 71335-0849 – Alprazolam

Alprazolam .5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-0849

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
71335-0849-010 TABLET in 1 BOTTLE (71335-0849-0)May 2, 2022
71335-0849-115 TABLET in 1 BOTTLE (71335-0849-1)Jun 20, 2018
71335-0849-230 TABLET in 1 BOTTLE (71335-0849-2)Jun 8, 2018
71335-0849-320 TABLET in 1 BOTTLE (71335-0849-3)May 2, 2022
71335-0849-4100 TABLET in 1 BOTTLE (71335-0849-4)May 2, 2022
71335-0849-590 TABLET in 1 BOTTLE (71335-0849-5)Sep 6, 2018
71335-0849-660 TABLET in 1 BOTTLE (71335-0849-6)Jun 8, 2018
71335-0849-7120 TABLET in 1 BOTTLE (71335-0849-7)May 2, 2022
71335-0849-828 TABLET in 1 BOTTLE (71335-0849-8)May 2, 2022
71335-0849-92 TABLET in 1 BOTTLE (71335-0849-9)Jun 22, 2018

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