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

Hailey Fe 1.5/30

CompanyGlenmark Pharmaceuticals Inc., USA (DUNS: 130597813)

Effective Date

February 21, 2023

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Manufacturing Establishments (1)

Glenmark Pharmaceuticals Limited

Labeler

Glenmark Pharmaceuticals Inc., USA

DUNS Number

677318665

Products (1)

Hailey Fe 1.5/30

NDC Product Code

68462-503

Application Number

ANDA209031

Marketing Category

ANDA (C73584)

Effective Date

February 21, 2023

© Copyright 2025. All Rights Reserved by MedPath

Home Terms & Conditions Privacy Policy