Omidria (Omeros Corporation)


Welcome to the PulseAid listing for the Omidria drug offered from Omeros Corporation. This alpha-1 Adrenergic Agonist [EPC],Adrenergic alpha1-Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Cyclooxygenase Inhibitor [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Omeros Corporation
NON-PROPRIETARY NAME: phenylephrine and ketorolac
SUBSTANCE NAME: PHENYLEPHRINE; KETOROLAC
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: alpha-1 Adrenergic Agonist [EPC],Adrenergic alpha1-Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Cyclooxygenase Inhibitor [EPC]
ROUTE: INTRAOCULAR
DOSAGE FORM: INJECTION, SOLUTION, CONCENTRATE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2014-06-13
END MARKETING DATE: 0000-00-00


Omidria HUMAN PRESCRIPTION DRUG Details:

Item DescriptionOmidria from Omeros Corporation
LABELER NAME: Omeros Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 10.16; 2.88(mg/mL; mg/mL)
START MARKETING DATE: 2014-06-13
END MARKETING DATE: 0000-00-00
PRODUCT ID: 62225-600_39475819-b338-1dd0-e054-00144ff8d46c
PRODUCT NDC: 62225-600
APPLICATION NUMBER: NDA205388

Other PHENYLEPHRINE; KETOROLAC Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Omeros CorporationOmidria