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Generated: September 24, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 085606

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NDA 085606 describes DEXAMETHASONE SODIUM PHOSPHATE, which is a drug marketed by Mylan Labs Ltd, Watson Labs, West-ward Pharms Int, Fresenius Kabi Usa, Intl Medication, Teva Parenteral, Luitpold, Wyeth Ayerst, Bel Mar, Akorn, Dell Labs, Lyphomed, Bausch And Lomb, Sola Barnes Hind, Sandoz Inc, and Aurobindo Pharma Ltd, and is included in twenty-eight NDAs. It is available from twenty-one suppliers. Additional details are available on the DEXAMETHASONE SODIUM PHOSPHATE profile page.

The generic ingredient in DEXAMETHASONE SODIUM PHOSPHATE is dexamethasone sodium phosphate. There are thirty-nine drug master file entries for this compound. Twenty-two suppliers are listed for this compound. Additional details are available on the dexamethasone sodium phosphate profile page.

Summary for NDA: 085606

Summary for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrengthEQ 24MG PHOSPHATE/ML
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No


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Serving 500+ biopharmaceutical companies globally:

Teva
Fuji
Cipla
Dow
Harvard Business School
Healthtrust
Express Scripts
UBS
McKinsey
Colorcon

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