TREXIMET (GlaxoSmithKline LLC)


Welcome to the PulseAid listing for the TREXIMET drug offered from GlaxoSmithKline LLC. This Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [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: GlaxoSmithKline LLC
NON-PROPRIETARY NAME: sumatriptan and naproxen sodium
SUBSTANCE NAME: SUMATRIPTAN SUCCINATE; NAPROXEN SODIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2008-04-25
END MARKETING DATE: 2018-07-31


TREXIMET HUMAN PRESCRIPTION DRUG Details:

Item DescriptionTREXIMET from GlaxoSmithKline LLC
LABELER NAME: GlaxoSmithKline LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 85; 500(mg/1; mg/1)
START MARKETING DATE: 2008-04-25
END MARKETING DATE: 2018-07-31
PRODUCT ID: 0173-0750_33607e05-3cfe-4e44-9a3b-aec5d2062c8e
PRODUCT NDC: 0173-0750
APPLICATION NUMBER: NDA021926

Other SUMATRIPTAN SUCCINATE; NAPROXEN SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
GlaxoSmithKline LLCTREXIMET
Pernix TherapeuticsTreximet
Rebel Distributors CorpTREXIMET