NDC 61145-101

Diclofenac SodiumDelayed Release 50 mg tablet, delayed release

On the label: RePharm Pharmaceuticals. It's repackaged: RePharm Pharmaceuticals rebottles it from Carlsbad Technology, Inc.'s NDC 61442-102.

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

Repackaging site

Product details

Generic drug
Diclofenac: every company that makes it
Form
tablet, delayed release
Strength
50 mg
Approval
ANDA ANDA075185
On the market since
Sep 27, 2017
Package NDCs
61145-101-06 61145-101-09 61145-101-18
Official label
DailyMed (National Library of Medicine), updated Nov 12, 2025

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