NDC 0121-0670

Ethosuximide 250 mg per 5 mL solution

On the label: Pharmaceutical Associates, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI PharmaGreenville, SC, United StatesMakes it No problems foundAug 1, 2025 · 18 inspections, 1 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
Ethosuximide: every company that makes it
Form
solution, oral
Strength
250 mg per 5 mL
Approval
ANDA ANDA040253
On the market since
Nov 22, 2000
Package NDCs
0121-0670-16
Official label
DailyMed (National Library of Medicine), updated Oct 17, 2025

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