NDC 49999-046

Orphenadrine Citrate 100 mg tablet, extended release

On the label: Lake Erie Medical DBA Quality Care Products LLC. It's repackaged: Lake Erie Medical DBA Quality Care Products LLC rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 43386-480.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Novel Laboratories, Inc.Somerset, NJ, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Orphenadrine: every company that makes it
Form
tablet, extended release, oral
Strength
100 mg
Approval
ANDA ANDA040284
On the market since
Feb 7, 2011
Package NDCs
49999-046-14 49999-046-30 49999-046-60 49999-046-90
Official label
DailyMed (National Library of Medicine), updated Dec 16, 2024

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