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Serving 500+ biopharmaceutical companies globally:

Cerilliant
Citi
Johnson and Johnson
Queensland Health
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Daiichi Sankyo
Covington
US Army
Dow
Boehringer Ingelheim

Generated: August 22, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 073591

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NDA 073591 describes LACTULOSE, which is a drug marketed by Morton Grove, Fresenius Kabi, Solvay, Apotex Inc, Cumberland Pharms, Pharm Assoc, Ani Pharms, Paco, Vistapharm, Bio-pharm Inc, Hi Tech Pharma, Roxane, West-ward Pharms Int, and Vintage Pharms, and is included in twenty NDAs. It is available from nineteen suppliers. Additional details are available on the LACTULOSE profile page.

The generic ingredient in LACTULOSE is lactulose. There are twenty drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the lactulose profile page.

Summary for NDA: 073591

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:0
Therapeutic Class:Gastrointestinal Agents
Formulation / Manufacturing:see details

Pharmacology for NDA: 073591

Suppliers and Packaging for NDA: 073591

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
LACTULOSE
lactulose
SOLUTION;ORAL 073591 ANDA West-Ward Pharmaceuticals Corp. 0054-3486 0054-3486-63 500 mL in 1 BOTTLE, PLASTIC (0054-3486-63)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:SOLUTION;ORALStrength10GM/15ML
Approval Date:May 29, 1992TE:AARLD:No


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Serving 500+ biopharmaceutical companies globally:

Daiichi Sankyo
Merck
Express Scripts
Chubb
Federal Trade Commission
Farmers Insurance
Chinese Patent Office
US Department of Justice
QuintilesIMS
AstraZeneca

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