NDC 59762-2350

Ethosuximide 250 mg per 5 mL solution

On the label: Mylan Pharmaceuticals Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Pharmacia & Upjohn Company LLCKalamazoo, MI, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections

Product details

Generic drug
Ethosuximide: every company that makes it
Form
solution, oral
Strength
250 mg per 5 mL
Approval
ANDA ANDA080258
On the market since
Feb 21, 2020
Package NDCs
59762-2350-6 59762-2350-7
Official label
DailyMed (National Library of Medicine), updated Jul 24, 2026

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