Class II ยท Moderate risk
Neoral soft gelatin capsules
CGMP deviations: Out of specification results obtained during routine stability testing for ethanol content.
National Drug Code
Is NDC 0078-0246-15 recalled?
Neoral · 30 BLISTER PACK in 1 CARTON (0078-0246-15) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0078-0246-61)
Yes — this exact package was recalled
1 FDA recall names the code 0078-0246-15 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
- cyclosporine
- Strength
- CYCLOSPORINE 25 mg/1
- Form
- Capsule, Liquid Filled · Oral
- Labeler
- Novartis Pharmaceuticals Corporation
- Type
- Human Prescription Drug
- Product code
- 0078-0246
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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