Prednisolone Acetate 68071-2222-05

Package NDC

68071-2222-05

Manufacturer: Nucare Pharmaceuticals,inc.
Dosage Form: Suspension/ Drops
Route: Ophthalmic
Product Type: Human Prescription Drug
Marketing Start: August 19, 1997
Listing Expires: December 31, 2026
Application: NDA017011

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Active Ingredients

Ingredient	Strength
Prednisolone Acetate	10 mg/mL

Drug Class

Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]

Selected Package

68071-2222-05Selected

1 BOTTLE, DROPPER in 1 CARTON (68071-2222-5) / 5 mL in 1 BOTTLE, DROPPER