NDC 76420-242
Baclofen 20 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-395.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Mahabubnagar, India | Makes it and tests it | No problems foundJan 18, 2023 · 2 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it
Product details
- Generic drug
- Baclofen: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA214099
- On the market since
- Jul 13, 2021
- Package NDCs
76420-242-1276420-242-3076420-242-6076420-242-90- Official label
- DailyMed (National Library of Medicine), updated Jan 15, 2025
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