NDC 71335-1892 – Aripiprazole

Aripiprazole 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1892

Product details

Brand name
Aripiprazole
Generic name
Aripiprazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205064
Marketed since
April 28, 2015
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Aripiprazole →

Package NDC codes (4)

Package NDCDescriptionSince
71335-1892-130 TABLET in 1 BOTTLE (71335-1892-1)Jun 29, 2021
71335-1892-228 TABLET in 1 BOTTLE (71335-1892-2)Jun 29, 2021
71335-1892-390 TABLET in 1 BOTTLE (71335-1892-3)Jun 29, 2021
71335-1892-460 TABLET in 1 BOTTLE (71335-1892-4)Jun 29, 2021

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