Class III ยท Low risk
Lamotrigine Tablets
Presence of Foreign Substance consistent with granules from desiccant packs used during storage
National Drug Code
Is NDC 42291-0368-60 recalled?
Lamotrigine · 60 TABLET in 1 BOTTLE (42291-368-60)
Yes — this exact package was recalled
1 FDA recall names the code 42291-0368-60 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Lamotrigine
- Strength
- LAMOTRIGINE 150 mg/1
- Form
- Tablet · Oral
- Labeler
- AvKARE
- Type
- Human Prescription Drug
- Product code
- 42291-0368
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 42291-0297 See recall 1
- 42291-0367 Lamotrigine 1
- 42291-0459 See recall 1
- 42291-0460 See recall 1
- 42291-0461 See recall 1
- 42291-0564 See recall 1
Free recall alerts
Know the day your medication is recalled
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