NDC 68001-232

Diclofenac Sodium and Misoprostol 75 mg / 200 ug tablet, delayed release

On the label: BluePoint Laboratories..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Actavis Laboratories FL, Inc.Davie, FL, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyNov 18, 2025 · 9 inspections, 2 with FDA action

Product details

Generic drug
Diclofenac and Misoprostol: every company that makes it
Form
tablet, delayed release, oral
Strength
75 mg / 200 ug
Approval
ANDA ANDA201089
On the market since
Feb 26, 2014
Package NDCs
68001-232-06
Official label
DailyMed (National Library of Medicine), updated Sep 11, 2025

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