NDC 51655-307 – Sulfamethoxazole and Trimethoprim

Sulfamethoxazole 800 mg/1; Trimethoprim 160 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC51655-307

Product details

Brand name
Sulfamethoxazole and Trimethoprim
Generic name
Sulfamethoxazole and Trimethoprim
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076899
Marketed since
November 17, 2022
Listing expires
December 31, 2027
Pharmacologic class
Dihydrofolate Reductase Inhibitor Antibacterial; Sulfonamide Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Sulfamethoxazole and Trimethoprim →

Package NDC codes (5)

Package NDCDescriptionSince
51655-307-2020 TABLET in 1 BOTTLE, PLASTIC (51655-307-20)Nov 17, 2022
51655-307-2928 TABLET in 1 BOTTLE, PLASTIC (51655-307-29)Feb 3, 2023
51655-307-5310 TABLET in 1 BOTTLE, PLASTIC (51655-307-53)Jan 2, 2023
51655-307-8414 TABLET in 1 BOTTLE, PLASTIC (51655-307-84)Nov 17, 2022
51655-307-876 TABLET in 1 BOTTLE, PLASTIC (51655-307-87)Jan 12, 2023

Recalls mentioning this NDC

Other Sulfamethoxazole and Trimethoprim products