NDC 67046-117

Cyclobenzaprine Hydrochloride 10 mg tablet, film coated

On the label: Coupler Enterprises Inc.. It's repackaged: Coupler Enterprises Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-007.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Kvk-Tech, Inc.Newtown, PA, United StatesMakes it Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action

Repackaging site

Product details

Generic drug
Cyclobenzaprine: every company that makes it
Form
tablet, film coated
Strength
10 mg
Approval
ANDA ANDA078048
On the market since
Sep 28, 2017
Package NDCs
67046-117-07 67046-117-14 67046-117-15 67046-117-20 67046-117-21 67046-117-28 67046-117-30 67046-117-60
Official label
DailyMed (National Library of Medicine), updated Sep 28, 2017

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