NDC 77771-182

Hydralazine Hydrochloride 10 mg tablet

On the label: Radha Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it and tests it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Hydralazine: every company that makes it
Form
tablet, oral
Strength
10 mg
Approval
ANDA ANDA205236
On the market since
Mar 4, 2021
Package NDCs
77771-182-01 77771-182-10
Official label
DailyMed (National Library of Medicine), updated Mar 12, 2021

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