NDC 68382-800

Labetalol Hydrochloride 300 mg tablet, film coated

On the label: Zydus Pharmaceuticals (USA) Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections

Product details

Generic drug
Labetalol: every company that makes it
Form
tablet, film coated, oral
Strength
300 mg
Approval
ANDA ANDA207743
On the market since
Dec 5, 2017
Package NDCs
68382-800-01 68382-800-05 68382-800-06 68382-800-16
Official label
DailyMed (National Library of Medicine), updated Mar 2, 2026

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