United States · FDA National Drug Code directory

aripiprazole

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
13668-217_264dc32a-9f5f-43be-96ee-0d30503de683
Product NDC
13668-217
Form
TABLET
Composition / generic term
aripiprazole
Labeler
Torrent Pharmaceuticals Limited
Marketing category
ANDA
Marketing start / end (source format)
20150428
Source listing expiry
20261231

Source-listed ingredients

  • ARIPIPRAZOLE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (13668-217-01) · 13668-217-01
  • 500 TABLET in 1 BOTTLE (13668-217-05) · 13668-217-05
  • 30 TABLET in 1 BOTTLE (13668-217-30) · 13668-217-30
  • 6250 TABLET in 1 BOTTLE (13668-217-69) · 13668-217-69
  • 90 TABLET in 1 BOTTLE (13668-217-90) · 13668-217-90

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →