NDC 67296-0709
Orphenadrine Citrate 100 mg tablet, extended release
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. 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
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Orphenadrine: every company that makes it
- Form
- tablet, extended release
- Strength
- 100 mg
- Approval
- ANDA ANDA040284
- On the market since
- Jun 19, 1998
- Package NDCs
67296-0709-167296-0709-2- Official label
- DailyMed (National Library of Medicine), updated Jul 11, 2024
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