Clinical Trials

Find trials by condition, location & phase

Drug Monographs

Browse drug monographs and information

Explore organizations and their profiles

Latest updates on trials and healthcare

Approved products by global authorities

AI-Powered Research

Discover powerful insights with advanced AI analysis tools for clinical trials.

Premium Access

Get unlimited access to our comprehensive pharmaceutical database and analytics.

FDA Approval

Sulfamethoxazole and Trimethoprim

CompanyNorthwind Pharmaceuticals (DUNS: 036986393)

Effective Date

November 10, 2014

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Trimethoprim(160 mg in 1 1)

Sulfamethoxazole(800 mg in 1 1)

Registrants (1)

Northwind Pharmaceuticals

DUNS Number

036986393

Manufacturing Establishments (1)

Northwind Pharmaceuticals

Labeler

Northwind Pharmaceuticals

Registrant

Northwind Pharmaceuticals

DUNS Number

036986393

Products (1)

Sulfamethoxazole and Trimethoprim

NDC Product Code

51655-111

Application Number

ANDA076817

Marketing Category

ANDA (C73584)

Route of Administration

ORAL

Effective Date

November 10, 2014

Ingredients

TrimethoprimActive

Code: AN164J8Y0XClass: ACTIBQuantity: 160 mg in 1 1

SulfamethoxazoleActive

Code: JE42381TNVClass: ACTIBQuantity: 800 mg in 1 1

© Copyright 2025. All Rights Reserved by MedPath

Home Terms & Conditions Privacy Policy