NDC 61442-102

Diclofenac SodiumDelayed Release 50 mg tablet, delayed release

On the label: Carlsbad Technology, Inc..

United States: 1

Where it's 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
50 mg
Approval
ANDA ANDA075185
On the market since
Nov 13, 1998
Package NDCs
61442-102-01 61442-102-10 61442-102-60
Official label
DailyMed (National Library of Medicine), updated May 28, 2025

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