United States · FDA National Drug Code directory
esmolol 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
- 55150-421_5aebd586-47c6-4e19-88e3-ef0ecb1cc875
- Product NDC
- 55150-421
- Form
- INJECTION
- Composition / generic term
- esmolol hydrochloride in sodium chloride
- Labeler
- Eugia US LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220321
- Source listing expiry
- 20261231
Source-listed ingredients
- ESMOLOL HYDROCHLORIDE — 20 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 POUCH in 1 CARTON (55150-421-10) / 1 BAG in 1 POUCH (55150-421-01) / 100 mL in 1 BAG · 55150-421-10
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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