United States · FDA National Drug Code directory
Eptifibatide
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
- 55150-219_944b269c-d810-411d-9ed4-8edd9d0ac1b7
- Product NDC
- 55150-219
- Form
- INJECTION
- Composition / generic term
- Eptifibatide
- Labeler
- Eugia US LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151208
- Source listing expiry
- 20261231
Source-listed ingredients
- EPTIFIBATIDE — 20 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-DOSE in 1 CARTON (55150-219-10) / 10 mL in 1 VIAL, SINGLE-DOSE · 55150-219-10
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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