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FDA ANDA · ANDA204962

PREDNISOLONE SODIUM PHOSPHATE

Sponsor: PHARM ASSOC

APPLICATION
ANDA204962
TYPE
ANDA
ORIGINAL APPROVAL
2020-03-11
LATEST ACTION
2024-06-05
ROUTE
ORAL
DOSAGE FORM
SOLUTION
MARKETING STATUS
Discontinued

Products

PREDNISOLONE SODIUM PHOSPHATEDiscontinued
PREDNISOLONE SODIUM PHOSPHATE EQ 30MG BASE/5ML · SOLUTION · ORAL

Approval history

2024-06-05Labeling · Supplement 2 · standardAP
2020-03-11UNKNOWN · OriginalLetterAP
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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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