NDC 71335-1894 – Alprazolam

Alprazolam 2 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-1894

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 (7)

Package NDCDescriptionSince
71335-1894-130 TABLET in 1 BOTTLE (71335-1894-1)Jun 29, 2021
71335-1894-260 TABLET in 1 BOTTLE (71335-1894-2)Jun 29, 2021
71335-1894-390 TABLET in 1 BOTTLE (71335-1894-3)Jun 29, 2021
71335-1894-4100 TABLET in 1 BOTTLE (71335-1894-4)Jun 29, 2021
71335-1894-510 TABLET in 1 BOTTLE (71335-1894-5)Jun 29, 2021
71335-1894-6120 TABLET in 1 BOTTLE (71335-1894-6)Jun 29, 2021
71335-1894-740 TABLET in 1 BOTTLE (71335-1894-7)Jun 29, 2021

Other Alprazolam products