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US Department of Justice
Merck
Cipla
McKinsey
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US Army
Johnson and Johnson
Chinese Patent Office
Boehringer Ingelheim

Generated: April 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 076895

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NDA 076895 describes PREDNISOLONE SODIUM PHOSPHATE, which is a drug marketed by Watson Labs, Akorn, Alcon Pharms Ltd, Bausch And Lomb, Sola Barnes Hind, Amneal Pharms, Chartwell Rx, Edenbridge Pharms, Hi Tech Pharma, Medicis Pharms, Mission Pharma, Nesher Pharms, Pharm Assoc, Vintage, Vintage Pharms, We Pharms, Wockhardt Bio Ag, and Mylan Pharms Inc, and is included in twenty-eight NDAs. It is available from fifteen suppliers. Additional details are available on the PREDNISOLONE SODIUM PHOSPHATE profile page.

The generic ingredient in PREDNISOLONE SODIUM PHOSPHATE is prednisolone sodium phosphate. There are eighty-six drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the prednisolone sodium phosphate profile page.
Pharmacology for NDA: 076895
Suppliers and Packaging for NDA: 076895
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
PREDNISOLONE SODIUM PHOSPHATE prednisolone sodium phosphate SOLUTION;ORAL 076895 ANDA A-S Medication Solutions 50090-0955 N 50090-0955-0
PREDNISOLONE SODIUM PHOSPHATE prednisolone sodium phosphate SOLUTION;ORAL 076895 ANDA Morton Grove Pharmaceuticals, Inc. 60432-212 N 60432-212-08

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:SOLUTION;ORALStrengthEQ 15MG BASE/5ML
Approval Date:Oct 4, 2004TE:AARLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Citi
Covington
UBS
Cantor Fitzgerald
AstraZeneca
Fuji
Colorcon
Medtronic
Farmers Insurance

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