NDC 71335-1832 – Aripiprazole

Aripiprazole 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1832

Product details

Brand name
Aripiprazole
Generic name
Aripiprazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207105
Marketed since
February 27, 2019
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Aripiprazole →

Package NDC codes (6)

Package NDCDescriptionSince
71335-1832-130 TABLET in 1 BOTTLE (71335-1832-1)Apr 29, 2021
71335-1832-228 TABLET in 1 BOTTLE (71335-1832-2)May 3, 2022
71335-1832-390 TABLET in 1 BOTTLE (71335-1832-3)Jun 24, 2021
71335-1832-460 TABLET in 1 BOTTLE (71335-1832-4)Jun 1, 2021
71335-1832-5120 TABLET in 1 BOTTLE (71335-1832-5)May 3, 2022
71335-1832-615 TABLET in 1 BOTTLE (71335-1832-6)May 3, 2022

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