NDC 42291-231

Diclofenac Sodium 75 mg tablet, delayed release

On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Carlsbad Technology, Inc.'s NDC 61442-103.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Carlsbad Technology, Inc.Carlsbad, CA, United StatesMakes it Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections

Product details

Generic drug
Diclofenac: every company that makes it
Form
tablet, delayed release, oral
Strength
75 mg
Approval
ANDA ANDA075185
On the market since
Mar 17, 2011
Package NDCs
42291-231-10 42291-231-18 42291-231-60
Official label
DailyMed (National Library of Medicine), updated Jan 14, 2026

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