Class II · Moderate risk
Desipramine Hydrochloride Tablets
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
National Drug Code
Is NDC 23155-0581-01 recalled?
Desipramine Hydrochloride · 100 TABLET in 1 BOTTLE (23155-581-01)
Yes — this exact package was recalled
1 FDA recall names the code 23155-0581-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- desipramine hydrochloride
- Strength
- DESIPRAMINE HYDROCHLORIDE 75 mg/1
- Form
- Tablet · Oral
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 23155-0581
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
- 23155-0110 See recall 3
- 23155-0645 See recall 3
- 23155-0646 See recall 3
- 23155-0216 Cidofovir Dihydrate 2
- 23155-0490 Desmopressin Acetate 2
- 23155-0002 See recall 1
Free recall alerts
Know the day your medication is recalled
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