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

MOXIFLOXACIN

CompanyDIRECT RX (DUNS: 079254320)

Effective Date

March 3, 2020

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Moxifloxacin(5 mg in 1 mL)

Registrants (1)

DUNS Number

079254320

Manufacturing Establishments (1)

Labeler

DIRECT RX

Registrant

DIRECT RX

DUNS Number

079254320

Products (1)

MOXIFLOXACIN

NDC Product Code

72189-076

Application Number

ANDA206242

Marketing Category

ANDA (C73584)

Route of Administration

OPHTHALMIC

Effective Date

March 3, 2020

Ingredients

MoxifloxacinActive

Code: C53598599TClass: ACTIMQuantity: 5 mg in 1 mL

HYDROCHLORIC ACIDInactive

Code: QTT17582CBClass: IACT

SODIUM CHLORIDEInactive

Code: 451W47IQ8XClass: IACT

BORIC ACIDInactive

Code: R57ZHV85D4Class: IACT

WATERInactive

Code: 059QF0KO0RClass: IACT

SODIUM HYDROXIDEInactive

Code: 55X04QC32IClass: IACT

© Copyright 2025. All Rights Reserved by MedPath

Home Terms & Conditions Privacy Policy