NDC 76420-880
Ramelteon 8 mg tablet, film coated
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-505.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Ramelteon: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 8 mg
- Approval
- ANDA ANDA215972
- On the market since
- Jul 10, 2023
- Package NDCs
76420-880-0176420-880-3076420-880-6076420-880-90- Official label
- DailyMed (National Library of Medicine), updated Jan 17, 2025
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