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Serving 500+ biopharmaceutical companies globally:

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Generated: June 29, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 091617

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NDA 091617 describes LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, which is a drug marketed by Alembic Pharms Ltd, Torrent Pharms, Aurobindo Pharma, West-ward Pharms Int, Cadista Pharms, Lupin Ltd, Sandoz, Apotex, Mylan, Teva Pharms, Watson Labs, Ipca Labs Ltd, Zydus Pharms Usa Inc, and Macleods Pharms Ltd, and is included in fourteen NDAs. It is available from forty-one suppliers. Additional details are available on the LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE profile page.

The generic ingredient in LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE 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: 091617

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:1
Formulation / Manufacturing:see details

Pharmacology for NDA: 091617

Ingredient-typeThiazides
Mechanism of ActionAngiotensin 2 Receptor Antagonists
Physiological EffectIncreased Diuresis

Suppliers and Packaging for NDA: 091617

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
hydrochlorothiazide; losartan potassium
TABLET;ORAL 091617 ANDA Qualitest Pharmaceuticals 0603-4228 0603-4228-02 90 TABLET, FILM COATED in 1 BOTTLE (0603-4228-02)
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
hydrochlorothiazide; losartan potassium
TABLET;ORAL 091617 ANDA Qualitest Pharmaceuticals 0603-4228 0603-4228-16 30 TABLET, FILM COATED in 1 BOTTLE (0603-4228-16)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength12.5MG;50MG
Approval Date:Feb 17, 2012TE:ABRLD:No

Summary for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength12.5MG;100MG
Approval Date:Feb 17, 2012TE:ABRLD:No

Summary for product number 003

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength25MG;100MG
Approval Date:Feb 17, 2012TE:ABRLD:No


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Serving 500+ biopharmaceutical companies globally:

Cantor Fitzgerald
Novartis
Chubb
Julphar
Daiichi Sankyo
Queensland Health
US Department of Justice
Johnson and Johnson
Mallinckrodt
Chinese Patent Office

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