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FDA ANDA · ANDA086754

MANNITOL 25%

Sponsor: ABRAXIS PHARM

APPLICATION
ANDA086754
TYPE
ANDA
ORIGINAL APPROVAL
1980-06-10
LATEST ACTION
1980-06-10
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued

Products

MANNITOL 25%Discontinued
MANNITOL 12.5GM/50ML · INJECTABLE · INJECTION

Approval history

1980-06-10OriginalAP
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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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