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
- 71335-2169_61f6ec35-0ee2-455a-a117-ef7a9d506342
- Product NDC
- 71335-2169
- Form
- TABLET, FILM COATED
- Composition / generic term
- Labetalol Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210818
- Source listing expiry
- 20271231
Source-listed ingredients
- LABETALOL HYDROCHLORIDE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-2169-1) · 71335-2169-1
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-2169-2) · 71335-2169-2
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-2169-3) · 71335-2169-3
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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