United States · FDA National Drug Code directory
Labetalol HCl in Sodium Chloride
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
- 0143-9364_d0e3d92d-d96e-4d5e-98ca-3d18a4bc82d8
- Product NDC
- 0143-9364
- Form
- INJECTION
- Composition / generic term
- LABETALOL HYDROCHLORIDE
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20201109
- Source listing expiry
- 20261231
Source-listed ingredients
- LABETALOL HYDROCHLORIDE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BAG in 1 BOX (0143-9364-10) / 200 mL in 1 BAG (0143-9364-01) · 0143-9364-10
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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