NDC 71335-1839 – Alprazolam

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

Human Prescription Drug DEA schedule CIV

Product NDC71335-1839

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
71335-1839-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1839-1)Apr 20, 2021
71335-1839-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1839-2)Mar 10, 2022
71335-1839-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1839-3)Mar 10, 2022
71335-1839-428 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1839-4)Mar 10, 2022
71335-1839-5120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1839-5)Mar 10, 2022

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