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

Is NDC 0904-2725-61 recalled?

Sulfamethoxazole and Trimethoprim · 100 BLISTER PACK in 1 CARTON (0904-2725-61) / 1 TABLET in 1 BLISTER PACK

Yes — this exact package was recalled

3 FDA recalls name the code 0904-2725-61 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.

2 of these recalls are still ongoing.

Active ingredient
Sulfamethoxazole and Trimethoprim
Strength
SULFAMETHOXAZOLE 800 mg/1; TRIMETHOPRIM 160 mg/1
Form
Tablet · Oral
Labeler
Major Pharmaceuticals
Type
Human Prescription Drug
Product code
0904-2725

Recalls naming this package

Class II · Moderate risk

Sulfamethoxazole and Trimethoprim

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 The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories NDC 55154-7895-0 D-0625-2025
Class II · Moderate risk

Sulfamethoxazole and Trimethoprim

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 The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories NDC 0904-2725-61 D-0624-2025

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