Class II · Moderate risk
Amlodipine Besylate Tablets
CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
National Drug Code
Is NDC 51079-0450-63 recalled?
Amlodipine Besylate Tablets
Yes — this exact package was recalled
1 FDA recall names the code 51079-0450-63 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.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
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
- 51079-0443 Levothyroxine Sodium 2
- 51079-0445 Levothyroxine Sodium 2
- 51079-0881 See recall 2
- 51079-0947 See recall 2
- 51079-0020 See recall 1
- 51079-0088 Mirtazapine 1
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