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Serving hundreds of leading biopharmaceutical companies globally:

Cantor Fitzgerald
Chubb
Merck
Federal Trade Commission
Teva
Dow
Julphar
Argus Health
McKinsey

Generated: April 20, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 075004

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NDA 075004 describes DILTIAZEM HYDROCHLORIDE, which is a drug marketed by Actavis Elizabeth, Actavis Labs Fl Inc, Apotex, Biovail, Mylan, Nesher Pharms, Par Pharm, Sandoz, Sun Pharm Inds Ltd, Sun Pharma Global, Teva, Valeant Pharms North, Zydus Pharms Usa Inc, Akorn Inc, Athenex Inc, Hikma Farmaceutica, Hospira, Intl Medication, Mylan Labs Ltd, Teva Pharms Usa, West-ward Pharms Int, Apothecon, Chartwell Molecules, Ivax Sub Teva Pharms, and Teva Pharms, and is included in thirty-six NDAs. It is available from forty-two suppliers. Additional details are available on the DILTIAZEM HYDROCHLORIDE profile page.

The generic ingredient in DILTIAZEM HYDROCHLORIDE is diltiazem hydrochloride. There are twenty-six drug master file entries for this compound. Forty-seven suppliers are listed for this compound. Additional details are available on the diltiazem hydrochloride profile page.
Summary for 075004
Tradename:DILTIAZEM HYDROCHLORIDE
Applicant:Hospira
Ingredient:diltiazem hydrochloride
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength5MG/ML
Approval Date:Feb 16, 2000TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Chubb
Accenture
Julphar
McKesson
Daiichi Sankyo
Fish and Richardson
Moodys
Argus Health
Harvard Business School

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