Product NDC: | 68788-9733 |
Proprietary Name: | PREDNISOLONE ACETATE |
Non Proprietary Name: | prednisolone acetate |
Active Ingredient(s): | 10 mg/mL & nbsp; prednisolone acetate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SUSPENSION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9733 |
Labeler Name: | Preferred Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017011 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20121023 |
Package NDC: | 68788-9733-5 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (68788-9733-5) > 5 mL in 1 BOTTLE, DROPPER |
NDC Code | 68788-9733-5 |
Proprietary Name | PREDNISOLONE ACETATE |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (68788-9733-5) > 5 mL in 1 BOTTLE, DROPPER |
Product NDC | 68788-9733 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | prednisolone acetate |
Dosage Form Name | SUSPENSION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20121023 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Preferred Pharmaceuticals, Inc. |
Substance Name | PREDNISOLONE ACETATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |