NDC 68071-3718

Diclofenac Potassium 50 mg tablet, film coated

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Archis Pharma LLC's NDC 72819-151.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Appco Pharma LLCPiscataway, NJ, United StatesMakes it Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections

Repackaging site

Product details

Generic drug
Diclofenac: every company that makes it
Form
tablet, film coated, oral
Strength
50 mg
Approval
ANDA ANDA075463
On the market since
Sep 15, 2021
Package NDCs
68071-3718-3
Official label
DailyMed (National Library of Medicine), updated Nov 11, 2024

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