Manage your pharmacy inventory

Project your formulary budget

Find generic entry opportunities

Anticipate generic drug launch

Deep knowledge on
small-molecule drugs and
the global patents
covering them

Drug patents …
… from Kazakhstan to Kalamazoo

BioPharmaceutical Business Intelligence

Analyze global market entry opportunities
Uncover prior art in expired and abandoned patents
Obtain formulation and manufacturing information

► See Plans & Pricing

Upgrade to enjoy subscriber-only features like email alerts and data export. See the Plans and Pricing

Serving 500+ biopharmaceutical companies globally:

Generated: September 19, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 090382

« Back to Dashboard

NDA 090382 describes LOSARTAN POTASSIUM, which is a drug marketed by Sandoz, Alembic Pharms Ltd, Watson Labs, Macleods Pharms Ltd, Unichem Labs Ltd, Lupin Ltd, Hetero Labs Ltd V, Micro Labs Ltd India, Zydus Pharms Usa Inc, Upsher-smith Labs, Teva, West-ward Pharms Int, Torrent Pharms, Cadista Pharms, Vivimed Global, Aurobindo Pharma, Apotex Corp, Ipca Labs Ltd, Mylan, Prinston Inc, Apotex, and Teva Pharms, and is included in thirty-five NDAs. It is available from sixty-seven suppliers. Additional details are available on the LOSARTAN POTASSIUM profile page.

The generic ingredient in LOSARTAN POTASSIUM is hydrochlorothiazide; losartan potassium. There are thirty-one drug master file entries for this compound. Forty-four suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; losartan potassium profile page.

Summary for NDA: 090382

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

Pharmacology for NDA: 090382

Mechanism of Action	Angiotensin 2 Receptor Antagonists

Suppliers and Packaging for NDA: 090382

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
LOSARTAN POTASSIUM	losartan potassium	TABLET;ORAL	090382	ANDA	Method Pharmaceuticals, LLC	58657-610	58657-610-10	1000 TABLET, FILM COATED in 1 BOTTLE (58657-610-10)
LOSARTAN POTASSIUM	losartan potassium	TABLET;ORAL	090382	ANDA	Method Pharmaceuticals, LLC	58657-610	58657-610-30	30 TABLET, FILM COATED in 1 BOTTLE (58657-610-30)

Summary for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	25MG
Approval Date:	Oct 6, 2010	TE:	AB	RLD:	No

Summary for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	50MG
Approval Date:	Oct 6, 2010	TE:	AB	RLD:	No

Summary for product number 003

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	100MG
Approval Date:	Oct 6, 2010	TE:	AB	RLD:	No

Complete Access Available with Subscription

For more information try a trial or see the database preview and plans and pricing

Serving 500+ biopharmaceutical companies globally:

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verifification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.