High Outlier
Strength
10 mg/mL
Manufacturer
Bausch & Lomb IncorporatedNDC
24208071510
Classification
Generic
Dosage Form
SOLUTION/ DROPS
Route
OPHTHALMIC
Last Updated
4/22/2026
Active Ingredients
PREDNISOLONE SODIUM PHOSPHATEApproval Type
Generic (ANDA)
FDA Application
ANDA040070On Market Since
7/29/1994
Pharmacological Classes
Corticosteroid Hormone Receptor Agonists
Corticosteroid
Generic Alternatives
No alternatives available
No alternatives found with the same active ingredient, strength, and dosage form.
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