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Serving leading biopharmaceutical companies globally:

QuintilesIMS
Argus Health
Accenture
Citi
Novartis
Healthtrust
Daiichi Sankyo
Colorcon
Johnson and Johnson
Boehringer Ingelheim

Generated: January 16, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 076870

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NDA 076870 describes ALLOPURINOL SODIUM, which is a drug marketed by West-ward Pharms Int and is included in one NDA. It is available from one supplier. Additional details are available on the ALLOPURINOL SODIUM profile page.

The generic ingredient in ALLOPURINOL SODIUM is allopurinol sodium. There are twenty-one drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the allopurinol sodium profile page.
Summary for 076870
Tradename:ALLOPURINOL SODIUM
Applicant:West-ward Pharms Int
Ingredient:allopurinol sodium
Patents:0
Formulation / Manufacturing:see details
Pharmacology for NDA: 076870
Mechanism of ActionXanthine Oxidase Inhibitors
Suppliers and Packaging for NDA: 076870
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
ALLOPURINOL SODIUM allopurinol sodium INJECTABLE;INJECTION 076870 ANDA West-Ward Pharmaceuticals Corp 0143-9533 0143-9533-01 1 VIAL in 1 BOX, UNIT-DOSE (0143-9533-01) > 25 mL in 1 VIAL

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 500MG BASE/VIAL
Approval Date:Aug 26, 2004TE:APRLD:No

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Serving leading biopharmaceutical companies globally:

Johnson and Johnson
Cantor Fitzgerald
Baxter
Daiichi Sankyo
McKinsey
Citi
Julphar
Mallinckrodt
Federal Trade Commission

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