NDC 71335-1364 – Aripiprazole

Aripiprazole 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1364

Product details

Brand name
Aripiprazole
Generic name
Aripiprazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203908
Marketed since
October 8, 2015
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Aripiprazole →

Package NDC codes (3)

Package NDCDescriptionSince
71335-1364-130 TABLET in 1 BOTTLE (71335-1364-1)Oct 4, 2019
71335-1364-228 TABLET in 1 BOTTLE (71335-1364-2)Oct 4, 2019
71335-1364-390 TABLET in 1 BOTTLE (71335-1364-3)Oct 4, 2019

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