NDC 0071-0525

Celontin 300 mg capsule

On the label: Parke-Davis Div of Pfizer Inc.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Pharmacia & Upjohn Company LLCKalamazoo, MI, United StatesMakes the active ingredient and tests it Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections
Pfizer Manufacturing Deutschland GmbHFreiburg im Breisgau, GermanyTests it Problems found, fixed voluntarilyJul 2, 2025 · 8 inspections

Product details

Generic drug
Methsuximide: every company that makes it
Form
capsule, oral
Strength
300 mg
Approval
NDA NDA010596
On the market since
Feb 8, 1957
Package NDCs
0071-0525-24
Official label
DailyMed (National Library of Medicine), updated Apr 7, 2026

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