NDC 87063-189
Ramelteon 8 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Micro Labs Limited's NDC 42571-375.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Micro Labs Limited | Verna, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 30, 2025 · 6 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, oral
- Strength
- 8 mg
- Approval
- ANDA ANDA215243
- On the market since
- May 1, 2023
- Package NDCs
87063-189-0187063-189-0587063-189-1087063-189-2087063-189-3087063-189-6087063-189-90- Official label
- DailyMed (National Library of Medicine), updated May 7, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?