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Generated: February 22, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 202747

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NDA 202747 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, Wockhardt Bio Ag, 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-three 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-five suppliers are listed for this compound. Additional details are available on the furosemide profile page.
Summary for 202747
Tradename:FUROSEMIDE
Applicant:Baxter Hlthcare Corp
Ingredient:furosemide
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details
Pharmacology for NDA: 202747
Medical Subject Heading (MeSH) Categories for 202747
Suppliers and Packaging for NDA: 202747
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
FUROSEMIDE furosemide INJECTABLE;INJECTION 202747 ANDA Baxter Healthcare Corporation 36000-063 N 36000-063-01
FUROSEMIDE furosemide INJECTABLE;INJECTION 202747 ANDA Baxter Healthcare Corporation 36000-064 N 36000-064-01

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrength10MG/ML
Approval Date:Jan 27, 2014TE:APRLD:No

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McKinsey
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