Class III · Low risk
Clonidine Hydrochloride Tablets
Failed Impurities/Degradation Specifications: potential migration of benzophenone at very low level into the product from container.
National Drug Code
Is NDC 29300-0135-01 recalled?
Clonidine Hydrochloride Tablets
Yes — this exact package was recalled
2 FDA recalls name the code 29300-0135-01 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
Class III · Low risk
Clonidine Hydrochloride Tablets
Failed Impurities/Degredation Specifications: This recall is initiated as a precautionary measure due to potential migration of Benzophenone at very low level into product from container label.
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
- 29300-0126 Bisoprolol Fumarate 2
- 29300-0128 Hydrochlorothiazide 2
- 29300-0113 Lamotrigine 1
- 29300-0116 topiramate 1
- 29300-0137 clonidine hydrochloride 1
- 29300-0140 Divalproex Sodium 1
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