NDC 71335-9666 – Alprazolam

Alprazolam .5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-9666

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 (10)

Package NDCDescriptionSince
71335-9666-010 TABLET in 1 BOTTLE (71335-9666-0)Mar 27, 2023
71335-9666-115 TABLET in 1 BOTTLE (71335-9666-1)Mar 27, 2023
71335-9666-230 TABLET in 1 BOTTLE (71335-9666-2)Mar 27, 2023
71335-9666-320 TABLET in 1 BOTTLE (71335-9666-3)Mar 27, 2023
71335-9666-4100 TABLET in 1 BOTTLE (71335-9666-4)Mar 27, 2023
71335-9666-590 TABLET in 1 BOTTLE (71335-9666-5)Mar 27, 2023
71335-9666-660 TABLET in 1 BOTTLE (71335-9666-6)Mar 27, 2023
71335-9666-7120 TABLET in 1 BOTTLE (71335-9666-7)Mar 27, 2023
71335-9666-828 TABLET in 1 BOTTLE (71335-9666-8)Mar 27, 2023
71335-9666-92 TABLET in 1 BOTTLE (71335-9666-9)Mar 27, 2023

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