Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 65862-0420-05 recalled?

Sulfamethoxazole and Trimethoprim · 500 TABLET in 1 BOTTLE (65862-420-05)

Yes — this exact package was recalled

2 FDA recalls name the code 65862-0420-05 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
Labeler
Aurobindo Pharma Limited
Type
Drug for Further Processing
Product code
65862-0420

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