Difluprednate Ophthalmic 00781-6000
Product NDC
00781-6000- 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 |
Packaging Options(1)
1 BOTTLE in 1 CARTON (0781-6000-78) / 5 mL in 1 BOTTLE