Product NDC: | 11980-180 |
Proprietary Name: | PRED FORTE |
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: | 11980-180 |
Labeler Name: | Allergan, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017011 |
Marketing Category: | NDA |
Start Marketing Date: | 19730601 |
Package NDC: | 11980-180-15 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (11980-180-15) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 11980-180-15 |
Proprietary Name | PRED FORTE |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (11980-180-15) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 11980-180 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | prednisolone acetate |
Dosage Form Name | SUSPENSION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 19730601 |
Marketing Category Name | NDA |
Labeler Name | Allergan, Inc. |
Substance Name | PREDNISOLONE ACETATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |