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
- 70771-1164_2be8d068-1830-4767-9e97-8d774d9a6001
- Product NDC
- 70771-1164
- Form
- TABLET, FILM COATED
- Composition / generic term
- Labetalol Hydrochloride
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171205
- Source listing expiry
- 20261231
Source-listed ingredients
- LABETALOL HYDROCHLORIDE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (70771-1164-1) · 70771-1164-1
- 30 TABLET, FILM COATED in 1 BOTTLE (70771-1164-3) · 70771-1164-3
- 500 TABLET, FILM COATED in 1 BOTTLE (70771-1164-5) · 70771-1164-5
- 90 TABLET, FILM COATED in 1 BOTTLE (70771-1164-9) · 70771-1164-9
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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