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Serving hundreds of leading biopharmaceutical companies globally:

Covington
Cantor Fitzgerald
Colorcon
Healthtrust
Mallinckrodt
Federal Trade Commission
Chubb
Merck
Express Scripts

Generated: April 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 084614

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NDA 084614 describes DEXAMETHASONE, which is a drug marketed by Alpharma Us Pharms, Lyne, Sti Pharma Llc, Vintage Pharms, Wockhardt Bio Ag, Abraxis Pharm, Fresenius Kabi Usa, West-ward Pharms Int, Watson Labs, ECR, Fera Pharms Llc, Idt Australia Ltd, Impax Labs, Larken Labs Inc, Par Pharm, Phoenix Labs Ny, Pvt Form, Roxane, Sun Pharm Industries, Upsher Smith, Whiteworth Town Plsn, Xspire Pharma, Watson Labs Teva, Akorn, Aurobindo Pharma Ltd, Bel Mar, Dell Labs, Intl Medication, Luitpold, Lyphomed, Mylan Labs Ltd, Teva Parenteral, Wyeth Ayerst, Sola Barnes Hind, Bausch And Lomb, and Sandoz Inc, and is included in seventy-eight NDAs. It is available from twenty-five suppliers. Additional details are available on the DEXAMETHASONE profile page.

The generic ingredient in DEXAMETHASONE is dexamethasone acetate. There are thirty-nine drug master file entries for this compound. Additional details are available on the dexamethasone acetate profile page.
Summary for 084614
Medical Subject Heading (MeSH) Categories for 084614

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength0.25MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Accenture
Johnson and Johnson
Deloitte
Mallinckrodt
Moodys
Fuji
Federal Trade Commission
Citi
Daiichi Sankyo

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