NDC 43063-407
Orphenadrine Citrate 100 mg tablet, extended release
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 43386-480.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Novel Laboratories, Inc. | Somerset, NJ, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
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
- Jun 19, 1998
- Package NDCs
43063-407-1443063-407-2043063-407-3043063-407-60- Official label
- DailyMed (National Library of Medicine), updated Jan 7, 2026
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