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Last Updated: December 23, 2024

Details for New Drug Application (NDA): 083051

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NDA 083051 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. Ten suppliers are listed for this compound. Additional details are available on the mannitol profile page.

Summary for 083051

Tradename:	MANNITOL 25%
Applicant:	Intl Medication
Ingredient:	mannitol
Patents:	0

Medical Subject Heading (MeSH) Categories for 083051

Diuretics, Osmotic
Sweetening Agents

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	12.5GM/50ML
Approval Date:	Approved Prior to Jan 1, 1982	TE:		RLD:	No

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