United States · FDA National Drug Code directory
Aprepitant
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
- 0781-2322_a194823e-5961-4bc0-b18f-2f63d3cbb9c6
- Product NDC
- 0781-2322
- Form
- CAPSULE
- Composition / generic term
- aprepitant
- Labeler
- Sandoz Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161227
- Source listing expiry
- 20261231
Source-listed ingredients
- APREPITANT — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 CAPSULE in 1 DOSE PACK (0781-2322-46) · 0781-2322-46
- 1 BLISTER PACK in 1 CARTON (0781-2322-68) / 6 CAPSULE in 1 BLISTER PACK (0781-2322-06) · 0781-2322-68
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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