Class II ยท Moderate risk
TORSEMIDE Tablet
Labeling: Label Mixup; TORSEMIDE Tablet, 10 mg may be potentially mislabeled as MEXILETINE HCL, Capsule, 200 mg, NDC 00093874001, Pedigree: AD25264_7, EXP: 5/3/2014.
National Drug Code
Is NDC 31722-0530-01 recalled?
Torsemide · 100 TABLET in 1 BOTTLE (31722-530-01)
Yes — this exact package was recalled
1 FDA recall names the code 31722-0530-01 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.
- Active ingredient
- Torsemide
- Strength
- TORSEMIDE 10 mg/1
- Form
- Tablet · Oral
- Labeler
- Camber Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 31722-0530
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
- 31722-0726 Montelukast Sodium 3
- 31722-0713 Pantoprazole Sodium 2
- 31722-0270 See recall 1
- 31722-0307 Ketorolac Tromethamine 1
- 31722-0513 Simvastatin 1
- 31722-0525 Finasteride 1
Free recall alerts
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