NDC 61919-177

Orphenadrine Citrate 100 mg tablet, extended release

On the label: Direct Rx. It's repackaged: Direct Rx 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
Strength
100 mg
Approval
ANDA ANDA040284
On the market since
Aug 29, 2019
Package NDCs
61919-177-72
Official label
DailyMed (National Library of Medicine), updated Jan 9, 2024

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