Home
>
National Drug Code (NDC)
>
PREDNISOLONE ACETATE
PREDNISOLONE ACETATE - 52125-484-01 - (prednisolone acetate)
Drug Information of PREDNISOLONE ACETATE
| Product NDC: | 52125-484 |
| Proprietary Name: | PREDNISOLONE ACETATE |
| Non Proprietary Name: | prednisolone acetate |
| Active Ingredient(s): | 10 mg/1 & nbsp; prednisolone acetate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SUSPENSION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PREDNISOLONE ACETATE
| Product NDC: | 52125-484 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017011 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130412 |
Package Information of PREDNISOLONE ACETATE
| Package NDC: | 52125-484-01 |
| Package Description: | 1 SUSPENSION/ DROPS in 1 CARTON (52125-484-01) |
NDC Information of PREDNISOLONE ACETATE
| NDC Code | 52125-484-01 |
| Proprietary Name | PREDNISOLONE ACETATE |
| Package Description | 1 SUSPENSION/ DROPS in 1 CARTON (52125-484-01) |
| Product NDC | 52125-484 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | prednisolone acetate |
| Dosage Form Name | SUSPENSION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20130412 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | PREDNISOLONE ACETATE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
