Evoxac (Daiichi Sankyo Pharma Development)


Welcome to the PulseAid listing for the Evoxac drug offered from Daiichi Sankyo Pharma Development. This Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [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: Daiichi Sankyo Pharma Development
NON-PROPRIETARY NAME: cevimeline hydrochloride
SUBSTANCE NAME: CEVIMELINE HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2000-01-12
END MARKETING DATE: 0000-00-00


Evoxac HUMAN PRESCRIPTION DRUG Details:

Item DescriptionEvoxac from Daiichi Sankyo Pharma Development
LABELER NAME: Daiichi Sankyo Pharma Development
DEA SCHEDULE:
ACTIVE STRENGTH: 30(mg/1)
START MARKETING DATE: 2000-01-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63395-201_3e7f5395-9fff-44d8-b44e-2c0e2c182f70
PRODUCT NDC: 63395-201
APPLICATION NUMBER: NDA020989

Other CEVIMELINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
American Health PackagingCevimeline Hydrochloride
Apotex Corp.Cevimeline Hydrochloride
Avera McKennan HospitalCevimeline Hydrochloride
Daiichi Sankyo Pharma DevelopmentEvoxac
Ingenus Pharmaceuticals NJ, LLCCEVIMELINE HYDROCHLORIDE
Ranbaxy Pharmaceuticals Inc.Cevimeline
Rising Pharmaceuticals, Inc.Cevimeline Hydrochloride
STAT RX USA LLCEVOXAC
West-Ward Pharmaceuticals Corp.Cevimeline Hydrochloride