Class II · Moderate risk
sulfaSALAzine
Labeling:Label Mixup; sulfaSALAzine Tablet, 500 mg may be potentially mislabeled as HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg, NDC 00574025001, Pedigree: AD46265_7, EXP: 5/15/2014.
National Drug Code
Is NDC 59762-5000-01 recalled?
Sulfasalazine
Yes — this exact package was recalled
1 FDA recall names the code 59762-5000-01 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
- Sulfasalazine
- Strength
- SULFASALAZINE 500 mg/1
- Form
- Tablet · Oral
- Labeler
- Mylan Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 59762-5000
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
- 59762-1415 See recall 2
- 59762-4538 See recall 2
- 59762-0068 Alprazolam XR 1
- 59762-0182 See recall 1
- 59762-0220 See recall 1
- 59762-0223 See recall 1
Free recall alerts
Know the day your medication is recalled
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