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
- 17856-0684_56433edd-6668-ea4e-e063-6294a90aa48e
- Product NDC
- 17856-0684
- Form
- SOLUTION
- Composition / generic term
- Aripiprazole oral
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231101
- Source listing expiry
- 20271231
Source-listed ingredients
- ARIPIPRAZOLE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0684-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-0684-3) · 17856-0684-1
- 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0684-2) / 10 mL in 1 CUP, UNIT-DOSE (17856-0684-4) · 17856-0684-2
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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