Class III ยท Low risk
Topiramate Tablets
Discoloration
National Drug Code
Is NDC 29300-0116-05 recalled?
topiramate · 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-116-05)
Yes — this exact package was recalled
1 FDA recall names the code 29300-0116-05 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
- topiramate
- Strength
- TOPIRAMATE 50 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Type
- Human Prescription Drug
- Product code
- 29300-0116
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
- 29300-0113 Lamotrigine 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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