Prednisolone Acetate 70748-0332
Product NDC
70748-0332- Manufacturer
- Lupin Pharmaceuticals, Inc.
- Dosage Form
- Suspension/ Drops
- Route
- Ophthalmic
- Product Type
- Human Prescription Drug
- Marketing Start
- October 11, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA216935
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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 in 1 CARTON (70748-332-02) / 5 mL in 1 BOTTLE
1 BOTTLE in 1 CARTON (70748-332-03) / 10 mL in 1 BOTTLE
1 BOTTLE in 1 CARTON (70748-332-04) / 15 mL in 1 BOTTLE