Product NDC: | 0065-1750 |
Proprietary Name: | ILEVRO |
Non Proprietary Name: | nepafenac |
Active Ingredient(s): | 3 mg/mL & nbsp; nepafenac |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0065-1750 |
Labeler Name: | Alcon Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA203491 |
Marketing Category: | NDA |
Start Marketing Date: | 20121220 |
Package NDC: | 0065-1750-07 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0065-1750-07) > 1.7 mL in 1 BOTTLE, DROPPER |
NDC Code | 0065-1750-07 |
Proprietary Name | ILEVRO |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0065-1750-07) > 1.7 mL in 1 BOTTLE, DROPPER |
Product NDC | 0065-1750 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nepafenac |
Dosage Form Name | SUSPENSION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20121220 |
Marketing Category Name | NDA |
Labeler Name | Alcon Laboratories, Inc. |
Substance Name | NEPAFENAC |
Strength Number | 3 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |