Class II · Moderate risk
DG Health Acid Reducer Ranitidine Tablets 150 mg
CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.
National Drug Code
Is NDC 55910-0092-79 recalled?
DG Health Acid Reducer Ranitidine Tablets 150 mg
Yes — this exact package was recalled
2 FDA recalls name the code 55910-0092-79 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.
2 of these recalls are still ongoing.
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
Ranitidine Tablets USP
CGMP DEVIATIONS: One lot of Ranitidine Tablets USP, 150 mg is being recalled because some bottles were empty.
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
- 55910-0852 See recall 2
- 55910-0011 See recall 1
- 55910-0183 citroma 1
- 55910-0251 DG Health Childrens Pain and Fever 1
- 55910-0419 See recall 1
- 55910-0423 See recall 1
Free recall alerts
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