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Generated: December 13, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 018667

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NDA 018667 describes FUROSEMIDE, which is a drug marketed by Abraxis Pharm, Accord Hlthcare, Amneal Pharms Co, Astrazeneca, Baxter Hlthcare Corp, Emcure Pharms Ltd, Fresenius Kabi Usa, Hospira, Igi Labs Inc, Intl Medication, Luitpold, Marsam Pharms Llc, Smith And Nephew, Warner Chilcott, Watson Labs, West-ward Pharms Int, Wockhardt, Wyeth Ayerst, Dava Pharms Inc, Ipca Labs Ltd, Ivax Sub Teva Pharms, Kalapharm, Leading Pharma Llc, Mylan, Prinston Inc, Sandoz, Sun Pharm Inds Inc, Sun Pharm Industries, Superpharm, and Watson Labs Teva, and is included in fifty-seven NDAs. It is available from sixty-two suppliers. Additional details are available on the FUROSEMIDE profile page.

The generic ingredient in FUROSEMIDE is furosemide. There are twenty-one drug master file entries for this compound. Sixty-four suppliers are listed for this compound. Additional details are available on the furosemide profile page.

Summary for 018667

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

Pharmacology for NDA: 018667

Medical Subject Heading (MeSH) Categories for 018667

Suppliers and Packaging for NDA: 018667

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
FUROSEMIDE furosemide INJECTABLE;INJECTION 018667 NDA Hospira, Inc. 0409-6102 0409-6102-25 25 VIAL, SINGLE-USE in 1 TRAY (0409-6102-25) > 2 mL in 1 VIAL, SINGLE-USE (0409-6102-35)
FUROSEMIDE furosemide INJECTABLE;INJECTION 018667 NDA Hospira, Inc. 0409-6102 0409-6102-26 25 VIAL, SINGLE-USE in 1 TRAY (0409-6102-26) > 4 mL in 1 VIAL, SINGLE-USE (0409-6102-36)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrength10MG/ML
Approval Date:May 28, 1982TE:APRLD:No


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Queensland Health

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