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FDA ANDA · ANDA218256

PREDNISOLONE ACETATE

Sponsor: AMNEAL

APPLICATION
ANDA218256
TYPE
ANDA
ORIGINAL APPROVAL
2025-06-11
LATEST ACTION
2025-06-11
ROUTE
OPHTHALMIC
DOSAGE FORM
SUSPENSION/DROPS
MARKETING STATUS
Prescription

Products

PREDNISOLONE ACETATEPrescription
PREDNISOLONE ACETATE 1% · SUSPENSION/DROPS · OPHTHALMIC

Approval history

2025-06-11UNKNOWN · Original · standardAP
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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