Class II ยท Moderate risk
Nifedipine
Labeling: Incorrect or Missing Lot and/or Exp Date: Greenstone LLC is recalling Nifedipine Extended Release tablets (90mg). The expiration date on the package is 48 months instead of 36 months.
National Drug Code
Is NDC 59762-6692-08 recalled?
Nifedipine
Yes — this exact package was recalled
1 FDA recall names the code 59762-6692-08 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
- 59762-1415 See recall 2
- 59762-4538 See recall 2
- 59762-0068 Alprazolam XR 1
- 59762-0182 See recall 1
- 59762-0220 See recall 1
- 59762-0223 See recall 1
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