NDC 76420-359
Baclofen 20 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from TruPharma LLC.'s NDC 52817-321.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Rubicon Research Limited | Thane, India | Makes it and tests it | No problems foundMar 8, 2024 · 5 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Baclofen: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA209102
- On the market since
- Apr 1, 2018
- Package NDCs
76420-359-0076420-359-0176420-359-0576420-359-3076420-359-6076420-359-90- Official label
- DailyMed (National Library of Medicine), updated Aug 13, 2025
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