FDA NDC
LAMICTAL XR
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 0173-0754
- Proprietary name
- LAMICTAL XR
- Nonproprietary name
- lamotrigine
- Labeler
- GlaxoSmithKline LLC
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Strength
- 25 mg/1
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