NDC 71335-1935 – Aripiprazole

Aripiprazole 15 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1935

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
71335-1935-130 TABLET in 1 BOTTLE (71335-1935-1)Aug 24, 2021
71335-1935-215 TABLET in 1 BOTTLE (71335-1935-2)Apr 8, 2024
71335-1935-328 TABLET in 1 BOTTLE (71335-1935-3)Apr 8, 2024
71335-1935-460 TABLET in 1 BOTTLE (71335-1935-4)Apr 8, 2024
71335-1935-590 TABLET in 1 BOTTLE (71335-1935-5)Jan 27, 2022
71335-1935-6120 TABLET in 1 BOTTLE (71335-1935-6)Apr 8, 2024

Other Aripiprazole products