NDC 85534-0022
Methocarbamol 750 mg tablet
On the label: Hawaii Repack, Inc.. It's repackaged: Hawaii Repack, Inc. rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-612.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Oxford Pharmaceuticals, LLC | Birmingham, AL, United States | Makes it | Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections |
Product details
- Generic drug
- Methocarbamol: every company that makes it
- Form
- tablet, oral
- Strength
- 750 mg
- Approval
- ANDA ANDA040489
- On the market since
- Aug 15, 2019
- Package NDCs
85534-0022-085534-0022-185534-0022-285534-0022-3- Official label
- DailyMed (National Library of Medicine), updated Jun 26, 2026
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