Class III ยท Low risk
Lamotrigine Tablets
Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the tablets.
National Drug Code
Is NDC 29300-0113-05 recalled?
Lamotrigine · 500 TABLET in 1 BOTTLE, PLASTIC (29300-113-05)
Yes — this exact package was recalled
1 FDA recall names the code 29300-0113-05 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
- Unichem Pharmaceuticals (USA), Inc.
- Type
- Human Prescription Drug
- Product code
- 29300-0113
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
- 29300-0126 Bisoprolol Fumarate 2
- 29300-0128 Hydrochlorothiazide 2
- 29300-0135 See recall 2
- 29300-0116 topiramate 1
- 29300-0137 clonidine hydrochloride 1
- 29300-0140 Divalproex Sodium 1
Free recall alerts
Know the day your medication is recalled
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