Difluprednate Ophthalmic 00781-6000-78

Package NDC

00781-6000-78

Manufacturer: Sandoz Inc
Dosage Form: Emulsion
Route: Ophthalmic
Product Type: Human Prescription Drug
Marketing Start: May 15, 2013
Listing Expires: December 31, 2026
Application: NDA022212

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Active Ingredients

Ingredient	Strength
Difluprednate	.5 mg/mL

Selected Package

00781-6000-78Selected

1 BOTTLE in 1 CARTON (0781-6000-78) / 5 mL in 1 BOTTLE