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MANNITOL 25%

NDA · New Drug Application · Sponsor: HOSPIRA · Approved 1967-12-22

Drug application

FDA Application #
NDA016269
Application type
New Drug Application
Brand name
MANNITOL 25%
Generic name
MANNITOL
Active ingredients
MANNITOL
Dosage form
INJECTABLE
Route
INJECTION
Marketing status
Discontinued
Sponsor
HOSPIRA
Manufacturer
Hospira, Inc.
First approval
1967-12-22

Source

Authoritative
Drugs@FDA application overview
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