Class II · Moderate risk
Propranolol Hydrochloride Tablets
Failed Tablet/Capsule Specification: Teva is recalling certain lots of Propanolol HCl Tablets, 10 mg due to the potential of some tablets not conforming to weight specification.
National Drug Code
Is NDC 50111-0467-03 recalled?
Propranolol Hydrochloride Tablets
Yes — this exact package was recalled
1 FDA recall names the code 50111-0467-03 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
- 50111-0433 See recall 2
- 50111-0647 Fluoxetine 2
- 50111-0648 Fluoxetine 2
- 50111-0327 Hydralazine Hydrochloride 1
- 50111-0328 Hydralazine Hydrochloride 1
- 50111-0441 See recall 1
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