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Farmers Insurance
Covington
Fuji
QuintilesIMS
Medtronic
Colorcon
Dow
Express Scripts
Deloitte

Generated: May 27, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 203129

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NDA 203129 describes DEXAMETHASONE SODIUM PHOSPHATE, which is a drug marketed by Akorn, Aurobindo Pharma Ltd, Bel Mar, Dell Labs, Fresenius Kabi Usa, Intl Medication, Luitpold, Lyphomed, Mylan Labs Ltd, Teva Parenteral, Watson Labs, West-ward Pharms Int, Wyeth Ayerst, Sola Barnes Hind, Bausch And Lomb, Sandoz Inc, and Somerset Theraps Llc, and is included in twenty-nine NDAs. It is available from twenty 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-four suppliers are listed for this compound. Additional details are available on the dexamethasone sodium phosphate profile page.
Pharmacology for NDA: 203129
Suppliers and Packaging for NDA: 203129
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DEXAMETHASONE SODIUM PHOSPHATE dexamethasone sodium phosphate INJECTABLE;INJECTION 203129 ANDA Fresenius Kabi USA, LLC 76045-106 N 76045-106-10

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 4MG PHOSPHATE/ML
Approval Date:Sep 30, 2015TE:APRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Baxter
Dow
Harvard Business School
US Army
Julphar
Fuji
Federal Trade Commission
AstraZeneca
Cantor Fitzgerald

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