NDC 10370-208
LamotrigineExtended-Release 200 mg tablet, film coated, extended release
On the label: ENDO USA, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants ENDO USA, Inc. names for other drugs.
Product details
- Generic drug
- Lamotrigine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA201374
- On the market since
- Jan 2, 2026
- Package NDCs
10370-208-11- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2026
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