Class II ยท Moderate risk
Aprepitant Capsule
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 0781-2321-06 recalled?
Aprepitant · 1 BLISTER PACK in 1 CARTON (0781-2321-06) / 1 CAPSULE in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 0781-2321-06 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
- Sandoz Inc
- Type
- Human Prescription Drug
- Product code
- 0781-2321
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
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