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
- 36000-320_219d4dec-02d1-4d4b-88fd-01b1dbad3abc
- Product NDC
- 36000-320
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Labetalol Hydrochloride
- Labeler
- Baxter Healthcare Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210126
- Source listing expiry
- 20261231
Source-listed ingredients
- LABETALOL HYDROCHLORIDE — 5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (36000-320-10) / 4 mL in 1 VIAL (36000-320-01) · 36000-320-10
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →