NDC 70518-3875
Lithium Carbonate 300 mg tablet, film coated, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-223.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Lithium Cation: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA091544
- On the market since
- Sep 26, 2023
- Package NDCs
70518-3875-0- Official label
- DailyMed (National Library of Medicine), updated Mar 19, 2026
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