Product NDC: | 0065-0002 |
Proprietary Name: | NEVANAC |
Non Proprietary Name: | nepafenac |
Active Ingredient(s): | 1 mg/mL & nbsp; nepafenac |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0065-0002 |
Labeler Name: | Alcon Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021862 |
Marketing Category: | NDA |
Start Marketing Date: | 20050906 |
Package NDC: | 0065-0002-03 |
Package Description: | 3 mL in 1 BOTTLE, PLASTIC (0065-0002-03) |
NDC Code | 0065-0002-03 |
Proprietary Name | NEVANAC |
Package Description | 3 mL in 1 BOTTLE, PLASTIC (0065-0002-03) |
Product NDC | 0065-0002 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nepafenac |
Dosage Form Name | SUSPENSION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20050906 |
Marketing Category Name | NDA |
Labeler Name | Alcon Laboratories, Inc. |
Substance Name | NEPAFENAC |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |