NDC 71335-1893 – Aripiprazole

Aripiprazole 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1893

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 (6)

Package NDCDescriptionSince
71335-1893-130 TABLET in 1 BOTTLE (71335-1893-1)Jun 30, 2021
71335-1893-228 TABLET in 1 BOTTLE (71335-1893-2)Apr 5, 2024
71335-1893-390 TABLET in 1 BOTTLE (71335-1893-3)Jul 16, 2021
71335-1893-460 TABLET in 1 BOTTLE (71335-1893-4)Jul 19, 2021
71335-1893-5120 TABLET in 1 BOTTLE (71335-1893-5)Apr 5, 2024
71335-1893-615 TABLET in 1 BOTTLE (71335-1893-6)Apr 5, 2024

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