NDC 68071-2222
PREDNISOLONE ACETATE
Prednisolone Acetate
PREDNISOLONE ACETATE is a Ophthalmic Suspension/ Drops in the Human Prescription Drug category. It is labeled and distributed by Nucare Pharmaceuticals,inc.. The primary component is Prednisolone Acetate.
| Product ID | 68071-2222_ab72cf3d-7661-41b1-e053-2995a90a7f44 |
| NDC | 68071-2222 |
| Product Type | Human Prescription Drug |
| Proprietary Name | PREDNISOLONE ACETATE |
| Generic Name | Prednisolone Acetate |
| Dosage Form | Suspension/ Drops |
| Route of Administration | OPHTHALMIC |
| Marketing Start Date | 1997-08-19 |
| Marketing Category | NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC |
| Application Number | NDA017011 |
| Labeler Name | NuCare Pharmaceuticals,Inc. |
| Substance Name | PREDNISOLONE ACETATE |
| Active Ingredient Strength | 10 mg/mL |
| Pharm Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |