Class II ยท Moderate risk
TOPIRAMATE Tablets 200 mg
Presence of Foreign Tablets: Presence of topiramate 100 mg tablets comingled with 200 mg tablets.
National Drug Code
Is NDC 68382-0141-14 recalled?
topiramate · 60 TABLET, FILM COATED in 1 BOTTLE (68382-141-14)
Yes — this exact package was recalled
1 FDA recall names the code 68382-0141-14 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
- topiramate
- Strength
- TOPIRAMATE 200 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 68382-0141
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
- 68382-0021 Venlafaxine 2
- 68382-0033 See recall 2
- 68382-0095 Carvedilol 2
- 68382-0099 Paroxetine 2
- 68382-0110 Bromocriptine mesylate 2
- 68382-0123 Amlodipine Besylate 2
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.