NDC 46708-258 – Aripiprazole

Aripiprazole 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC46708-258

Product details

Brand name
Aripiprazole
Generic name
Aripiprazole
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202101
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 (5)

Package NDCDescriptionSince
46708-258-10100 TABLET in 1 CARTON (46708-258-10)Apr 28, 2015
46708-258-3030 TABLET in 1 BOTTLE (46708-258-30)Apr 28, 2015
46708-258-31100 TABLET in 1 BOTTLE (46708-258-31)Apr 28, 2015
46708-258-71500 TABLET in 1 BOTTLE (46708-258-71)Apr 28, 2015
46708-258-911000 TABLET in 1 BOTTLE (46708-258-91)Apr 28, 2015

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