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
- 65862-661_8c97812b-1663-41cd-b80b-cff6be56d7e5
- Product NDC
- 65862-661
- Form
- TABLET
- Composition / generic term
- Aripiprazole
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151008
- Source listing expiry
- 20271231
Source-listed ingredients
- ARIPIPRAZOLE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (65862-661-01) · 65862-661-01
- 500 TABLET in 1 BOTTLE (65862-661-05) · 65862-661-05
- 30 TABLET in 1 BOTTLE (65862-661-30) · 65862-661-30
- 10 BLISTER PACK in 1 CARTON (65862-661-78) / 10 TABLET in 1 BLISTER PACK (65862-661-10) · 65862-661-78
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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