Class III ยท Low risk
Lamotrigine Tablets
Presence of Foreign Substance visually consistent with the silica granules present in the desiccant packs utilized during storage of the product.
National Drug Code
Is NDC 59746-0247-97 recalled?
Lamotrigine
Yes — this exact package was recalled
1 FDA recall names the code 59746-0247-97 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
- Jubilant Cadista Pharmacuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 59746-0247
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
- 59746-0001 See recall 5
- 59746-0284 Pantoprazole Sodium 5
- 59746-0122 Meclizine Hydrochloride 2
- 59746-0360 valsartan 2
- 59746-0363 See recall 2
- 59746-0003 See recall 1
Free recall alerts
Know the day your medication is recalled
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