Class II · Moderate risk
Sulfamethoxazole and Trimethoprim Tablets
Labeling: Label Mix up; product labeled to contain Sulfamethoxazole and Trimethoprim Tablets, 400 mg/80 mg instead of Sulfamethoxazole and Trimethoprim Tablets, 800 mg/160 mg
National Drug Code
Is NDC 53746-0272-01 recalled?
Sulfamethoxazole and Trimethoprim · 100 TABLET in 1 BOTTLE (53746-272-01)
Yes — this exact package was recalled
1 FDA recall names the code 53746-0272-01 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
- Sulfamethoxazole and Trimethoprim
- Strength
- SULFAMETHOXAZOLE 800 mg/1; TRIMETHOPRIM 160 mg/1
- Form
- Tablet · Oral
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Type
- Human Prescription Drug
- Product code
- 53746-0272
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
- 53746-0178 See recall 7
- 53746-0179 See recall 2
- 53746-0253 Ranitidine 1
- 53746-0254 Ranitidine 1
- 53746-0544 Primidone 1
Free recall alerts
Know the day your medication is recalled
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