NDC 63323-614

Hydralazine Hydrochloride 20 mg per 1 mL injection

On the label: Fresenius Kabi, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Fresenius Kabi USA, LLCMelrose Park, IL, United StatesMakes it and tests it Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Hydralazine: every company that makes it
Form
injection, intramuscular; intravenous
Strength
20 mg per 1 mL
Approval
ANDA ANDA040388
On the market since
Sep 5, 2001
Package NDCs
63323-614-16 63323-614-41
Official label
DailyMed (National Library of Medicine), updated Oct 7, 2026

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