Class II ยท Moderate risk
Pregabalin Capsules
Failed Tablet/Capsule Specifications: Out of Specification results for particle Size Distribution and Bulk Density of the Active Pharmaceutical Ingredient.
National Drug Code
Is NDC 47335-0687-88 recalled?
Pregabalin · 100 CAPSULE in 1 BOTTLE (47335-687-88)
Yes — this exact package was recalled
1 FDA recall names the code 47335-0687-88 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
- Pregabalin
- Strength
- PREGABALIN 50 mg/1
- Form
- Capsule · Oral
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug · DEA CV
- Product code
- 47335-0687
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
- 47335-0737 Bupropion hydrochloride 6
- 47335-0738 Bupropion hydrochloride 5
- 47335-0506 Cequa 4
- 47335-0063 Dofetilide 2
- 47335-0343 See recall 2
- 47335-0049 Doxorubicin Hydrochloride 1
Free recall alerts
Know the day your medication is recalled
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