NDC 71335-1669 – Alprazolam

Alprazolam .5 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-1669

Product details

Brand name
Alprazolam
Generic name
Alprazolam
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090871
Marketed since
June 7, 2011
Listing expires
December 31, 2027
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Alprazolam →

Package NDC codes (5)

Package NDCDescriptionSince
71335-1669-160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1669-1)May 12, 2021
71335-1669-230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1669-2)Feb 14, 2022
71335-1669-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1669-3)Jul 21, 2020
71335-1669-445 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1669-4)Feb 14, 2022
71335-1669-5120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1669-5)Feb 14, 2022

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