Rhopressa is a Ophthalmic; Topical Solution/ Drops in the Human Prescription Drug category. It is labeled and distributed by Aerie Pharmaceuticals, Inc.. The primary component is Netarsudil Mesylate.
Product ID | 70727-497_10ffc705-641e-4e75-8f2a-3a98cccbc471 |
NDC | 70727-497 |
Product Type | Human Prescription Drug |
Proprietary Name | Rhopressa |
Generic Name | Netarsudil |
Dosage Form | Solution/ Drops |
Route of Administration | OPHTHALMIC; TOPICAL |
Marketing Start Date | 2017-12-18 |
Marketing Category | NDA / NDA |
Application Number | NDA208254 |
Labeler Name | Aerie Pharmaceuticals, Inc. |
Substance Name | NETARSUDIL MESYLATE |
Active Ingredient Strength | 0 mg/mL |
Pharm Classes | Rho Kinase Inhibitor [EPC],Rho Kinase Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2017-12-18 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA208254 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2017-12-18 |
Marketing Category | NDA |
Application Number | NDA208254 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-12-18 |
Ingredient | Strength |
---|---|
NETARSUDIL MESYLATE | .2 mg/mL |
SPL SET ID: | 7d4f0e3a-5b86-4c43-982a-813b22ae7e22 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RHOPRESSA 86231355 5317370 Live/Registered |
Aerie Pharmaceuticals, Inc. 2014-03-25 |