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

Is NDC 51655-0307-20 recalled?

Sulfamethoxazole and Trimethoprim · 20 TABLET in 1 BOTTLE, PLASTIC (51655-307-20)

Yes — this exact package was recalled

1 FDA recall names the code 51655-0307-20 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
Sulfamethoxazole and Trimethoprim
Strength
SULFAMETHOXAZOLE 800 mg/1; TRIMETHOPRIM 160 mg/1
Form
Tablet · Oral
Labeler
Northwind Health Company, LLC
Type
Human Prescription Drug
Product code
51655-0307

Recalls naming this package

Class II ยท Moderate risk

Sulfamethoxazole and Trimethoprim Tablets

Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

Ongoing Particulate / foreign matter Northwind Pharmaceuticals LLC NDC 51655-307-87 D-0654-2025

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