NDC 71205-392 – Aripiprazole

Aripiprazole 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-392

Product details

Brand name
Aripiprazole
Generic name
Aripiprazole
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203908
Marketed since
October 8, 2015
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Aripiprazole →

Package NDC codes (3)

Package NDCDescriptionSince
71205-392-3030 TABLET in 1 BOTTLE (71205-392-30)Jan 30, 2020
71205-392-6060 TABLET in 1 BOTTLE (71205-392-60)Jan 30, 2020
71205-392-9090 TABLET in 1 BOTTLE (71205-392-90)Jan 30, 2020

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