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Serving leading biopharmaceutical companies globally:

Accenture
Teva
Novartis
Moodys
Cantor Fitzgerald
Medtronic
McKinsey
Daiichi Sankyo
QuintilesIMS
Cipla

Generated: December 15, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 204394

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NDA 204394 describes MINOCYCLINE HYDROCHLORIDE, which is a drug marketed by Aurobindo Pharma, Impax Labs, Sun Pharm Inds Inc, Torrent Pharma Inc, Watson Labs, Watson Labs Teva, Zydus Worldwide, Alkem Labs Ltd, Aurobindo Pharma Ltd, Barr Labs Inc, Impax Labs Inc, Lupin Ltd, Mylan Pharms Inc, Sandoz, Sidmak Labs India, Sun Pharm Inds Ltd, Zydus Pharms Usa Inc, Dr Reddys Labs Ltd, Par Pharm, Sun Pharm Industries, and Triax Pharms, and is included in twenty-four NDAs. It is available from forty-five suppliers. Additional details are available on the MINOCYCLINE HYDROCHLORIDE profile page.

The generic ingredient in MINOCYCLINE HYDROCHLORIDE is minocycline hydrochloride. There are thirteen drug master file entries for this compound. Fifty-four suppliers are listed for this compound. Additional details are available on the minocycline hydrochloride profile page.

Summary for 204394

Tradename:1
Applicant:1
Ingredient:1
Patents:0
Therapeutic Class:Antibacterials
Dental and Oral Agents
Formulation / Manufacturing:see details

Medical Subject Heading (MeSH) Categories for 204394

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrengthEQ 45MG BASE
Approval Date:Dec 30, 2015TE:ABRLD:No

Summary for product number 004

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrengthEQ 80MG BASE
Approval Date:Dec 30, 2015TE:ABRLD:No

Summary for product number 005

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrengthEQ 105MG BASE
Approval Date:Dec 30, 2015TE:ABRLD:No


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Serving leading biopharmaceutical companies globally:

UBS
AstraZeneca
Argus Health
Boehringer Ingelheim
Citi
Colorcon
Novartis
Teva
US Department of Justice
Moodys

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