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FDA ANDA · ANDA078988

PREDNISOLONE SODIUM PHOSPHATE

Sponsor: PHARM ASSOC

APPLICATION
ANDA078988
TYPE
ANDA
ORIGINAL APPROVAL
2008-06-09
LATEST ACTION
2024-06-05
ROUTE
ORAL
DOSAGE FORM
SOLUTION
MARKETING STATUS
Prescription

Products

PREDNISOLONE SODIUM PHOSPHATEPrescription
PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML · SOLUTION · ORAL

Approval history

2024-06-05Labeling · Supplement 11 · standardAP
2010-03-24Labeling · Supplement 5AP
2008-06-09OriginalAP
VIEW ON DRUGS@FDA ↗

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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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