NDC 71335-1513 – Aripiprazole

Aripiprazole 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1513

Product details

Brand name
Aripiprazole
Generic name
Aripiprazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206174
Marketed since
May 30, 2017
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Aripiprazole →

Package NDC codes (6)

Package NDCDescriptionSince
71335-1513-130 TABLET in 1 BOTTLE (71335-1513-1)Feb 20, 2020
71335-1513-228 TABLET in 1 BOTTLE (71335-1513-2)Feb 14, 2022
71335-1513-390 TABLET in 1 BOTTLE (71335-1513-3)Feb 14, 2022
71335-1513-460 TABLET in 1 BOTTLE (71335-1513-4)Feb 14, 2022
71335-1513-5120 TABLET in 1 BOTTLE (71335-1513-5)Feb 14, 2022
71335-1513-615 TABLET in 1 BOTTLE (71335-1513-6)Feb 14, 2022

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