Class III ยท Low risk
Aprepitant Capsules
Shortfill: Aprepitant capsules 40 mg is being recalled due to customer reports of missing capsule in the blister pack.
National Drug Code
Is NDC 68462-0583-40 recalled?
Aprepitant · 1 BLISTER PACK in 1 CARTON (68462-583-40) / 1 CAPSULE in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 68462-0583-40 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
- Aprepitant
- Strength
- APREPITANT 40 mg/1
- Form
- Capsule · Oral
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Type
- Human Prescription Drug
- Product code
- 68462-0583
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
- 68462-0164 Carvedilol 5
- 68462-0165 Carvedilol 4
- 68462-0248 See recall 4
- 68462-0357 Potassium Chloride 4
- 68462-0562 Diltiazem Hydrochloride 4
- 68462-0249 See recall 3
Free recall alerts
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