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

WARFARIN SODIUM

CompanyNorthwind Pharmaceuticals, LLC (DUNS: 036986393)

Effective Date

March 23, 2015

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Warfarin(4 mg in 1 1)

Registrants (1)

Northwind Pharmaceuticals, LLC

DUNS Number

036986393

Manufacturing Establishments (1)

Northwind Pharmaceuticals, LLC

Labeler

Northwind Pharmaceuticals, LLC

Registrant

Northwind Pharmaceuticals, LLC

DUNS Number

036986393

Products (1)

WARFARIN SODIUM

NDC Product Code

51655-282

Application Number

ANDA040663

Marketing Category

ANDA (C73584)

Route of Administration

ORAL

Effective Date

March 23, 2015

Ingredients

Code: 6153CWM0CLClass: ACTIBQuantity: 4 mg in 1 1

© Copyright 2025. All Rights Reserved by MedPath

Home Terms & Conditions Privacy Policy