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Serving hundreds of leading biopharmaceutical companies globally:

Cerilliant
Moodys
Accenture
Dow
AstraZeneca
Federal Trade Commission
Harvard Business School
Johnson and Johnson
Argus Health

Generated: April 23, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 005620

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NDA 005620 describes MANNITOL 25%, which is a drug marketed by Abraxis Pharm, Fresenius Kabi Usa, Hospira, Igi Labs Inc, Intl Medication, Luitpold, Merck, and Watson Labs, and is included in nine NDAs. It is available from four suppliers. Additional details are available on the MANNITOL 25% profile page.

The generic ingredient in MANNITOL 25% is mannitol. There are eighteen drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the mannitol profile page.
Summary for 005620
Tradename:MANNITOL 25%
Applicant:Merck
Ingredient:mannitol
Patents:0
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 005620

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength12.5GM/50ML
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

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