PRED FORTE is a Ophthalmic Suspension/ Drops in the Human Prescription Drug category. It is labeled and distributed by Allergan, Inc.. The primary component is Prednisolone Acetate.
Product ID | 11980-180_1d4ed928-64f7-45e5-870e-56732694168e |
NDC | 11980-180 |
Product Type | Human Prescription Drug |
Proprietary Name | PRED FORTE |
Generic Name | Prednisolone Acetate |
Dosage Form | Suspension/ Drops |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 1973-06-01 |
Marketing Category | NDA / NDA |
Application Number | NDA017011 |
Labeler Name | Allergan, 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 | 2020-12-31 |
Marketing Start Date | 1973-06-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA017011 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1973-06-01 |
Marketing Category | NDA |
Application Number | NDA017011 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1973-06-01 |
Marketing Category | NDA |
Application Number | NDA017011 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1973-06-01 |
Marketing Category | NDA |
Application Number | NDA017011 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1973-06-01 |
Marketing Category | NDA |
Application Number | NDA017011 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1973-06-01 |
Marketing Category | NDA |
Application Number | NDA017011 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1973-06-01 |
Ingredient | Strength |
---|---|
PREDNISOLONE ACETATE | 10 mg/mL |
SPL SET ID: | 00a5aa88-e361-4ea7-8922-530c738b726e |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
11980-180 | PRED FORTE | prednisolone acetate |
51672-1338 | Flo-Pred | Prednisolone Acetate |
0065-0638 | OMNIPRED | prednisolone acetate |
11980-174 | PRED MILD | prednisolone acetate |
50090-0559 | Prednisolone Acetate | Prednisolone Acetate |
50090-0561 | Prednisolone Acetate | Prednisolone Acetate |
50090-1912 | PREDNISOLONE ACETATE | prednisolone acetate |
50090-5275 | PREDNISOLONE ACETATE | prednisolone acetate |
52959-265 | PREDNISOLONE ACETATE | prednisolone acetate |
60758-119 | PREDNISOLONE ACETATE | prednisolone acetate |
61314-637 | Prednisolone Acetate | Prednisolone Acetate |
68071-1722 | PREDNISOLONE ACETATE | prednisolone acetate |
68071-2222 | PREDNISOLONE ACETATE | prednisolone acetate |
72189-055 | PREDNISOLONE ACETATE | PREDNISOLONE ACETATE |
76420-204 | PREDNISOLONE ACETATE | prednisolone acetate |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PRED FORTE 74289736 1756405 Live/Registered |
ALLERGAN, INC. 1992-06-25 |