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Serving leading biopharmaceutical companies globally:

Express Scripts
Cerilliant
Healthtrust
Mallinckrodt
Boehringer Ingelheim
Johnson and Johnson
Dow
Colorcon
Medtronic
Queensland Health

Generated: October 16, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 077437

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NDA 077437 describes MOXIFLOXACIN HYDROCHLORIDE, which is a drug marketed by Watson Labs Inc, Aurobindo Pharma Ltd, Mylan Pharms Inc, Teva Pharms Usa, Dr Reddys Labs Ltd, Crossmedika Sa, Torrent Pharms Ltd, Lupin Ltd, Fresenius Kabi Usa, Apotex Inc, Msn Labs Pvt Ltd, Novel Labs Inc, and Mylan Labs Ltd, and is included in fifteen NDAs. It is available from fourteen suppliers. Additional details are available on the MOXIFLOXACIN HYDROCHLORIDE profile page.

The generic ingredient in MOXIFLOXACIN HYDROCHLORIDE is moxifloxacin hydrochloride. There are eighteen drug master file entries for this compound. Thirty suppliers are listed for this compound. Additional details are available on the moxifloxacin hydrochloride profile page.

Summary for NDA: 077437

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:0
Therapeutic Class:Antibacterials
Formulation / Manufacturing:see details

Pharmacology for NDA: 077437

Ingredient-typeQuinolones

Suppliers and Packaging for NDA: 077437

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
MOXIFLOXACIN HYDROCHLORIDE
moxifloxacin hydrochloride
TABLET;ORAL 077437 ANDA Teva Pharmaceuticals USA, Inc. 0093-7387 0093-7387-56 30 TABLET, FILM COATED in 1 BOTTLE (0093-7387-56)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrengthEQ 400MG BASE
Approval Date:Feb 18, 2014TE:ABRLD:No


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Serving leading biopharmaceutical companies globally:

QuintilesIMS
Julphar
Colorcon
Healthtrust
Fish and Richardson
Covington
Cipla
Harvard Business School
Accenture
US Army

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