Prednisolone Acetate 61314-0637
Product NDC
61314-0637- Manufacturer
- Sandoz Inc
- Dosage Form
- Suspension/ Drops
- Route
- Ophthalmic
- Product Type
- Human Prescription Drug
- Marketing Start
- December 15, 1994
- Listing Expires
- December 31, 2026
- Application
- NDA017469
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Prednisolone Acetate | 10 mg/mL |
Drug Class
Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(3)
1 BOTTLE, PLASTIC in 1 CARTON (61314-637-05) / 5 mL in 1 BOTTLE, PLASTIC
1 BOTTLE, PLASTIC in 1 CARTON (61314-637-10) / 10 mL in 1 BOTTLE, PLASTIC
1 BOTTLE, PLASTIC in 1 CARTON (61314-637-15) / 15 mL in 1 BOTTLE, PLASTIC