United States · FDA National Drug Code directory
Labetalol 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
- 83301-0058_e49bc25a-e39e-469a-8372-bd28e2b1ca7f
- Product NDC
- 83301-0058
- Form
- INJECTION
- Composition / generic term
- Labetalol Hydrochloride
- Labeler
- Mullan Pharmaceutical Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251205
- Source listing expiry
- 20261231
Source-listed ingredients
- LABETALOL HYDROCHLORIDE — 100 mg/20mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, MULTI-DOSE in 1 CARTON (83301-0058-1) / 20 mL in 1 VIAL, MULTI-DOSE · 83301-0058-1
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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