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
- 68788-7063_5ef48246-f66f-4839-83df-0c0863b342ce
- Product NDC
- 68788-7063
- Form
- TABLET
- Composition / generic term
- aripiprazole
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180105
- Source listing expiry
- 20261231
Source-listed ingredients
- ARIPIPRAZOLE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (68788-7063-1) · 68788-7063-1
- 20 TABLET in 1 BOTTLE (68788-7063-2) · 68788-7063-2
- 30 TABLET in 1 CARTON (68788-7063-3) · 68788-7063-3
- 60 TABLET in 1 BOTTLE (68788-7063-6) · 68788-7063-6
- 90 TABLET in 1 BOTTLE (68788-7063-9) · 68788-7063-9
Source and coverage
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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.
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