United States · FDA National Drug Code directory
Ziprasidone Hydrochloride
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
- 68084-104_3d34b9a4-f85e-f66c-e063-6394a90a0518
- Product NDC
- 68084-104
- Form
- CAPSULE
- Composition / generic term
- Ziprasidone HCl
- Labeler
- American Health Packaging
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141217
- Source listing expiry
- 20261231
Source-listed ingredients
- ZIPRASIDONE HYDROCHLORIDE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 80 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-104-09) / 1 CAPSULE in 1 BLISTER PACK (68084-104-11) · 68084-104-09
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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