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MANNITOL 25%

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: FRESENIUS KABI USA · Approved 1972-08-11

Drug application

FDA Application #

ANDA080677

Application type

Abbreviated New Drug Application (Generic)

Brand name

MANNITOL 25%

Generic name

MANNITOL

Active ingredients

MANNITOL

Dosage form

INJECTABLE

Route

INJECTION

Marketing status

Prescription

Sponsor

FRESENIUS KABI USA

Manufacturer

Fresenius Kabi USA, LLC

First approval

1972-08-11

Source

Authoritative

Drugs@FDA application overview

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