Armodafinil (Actavis Pharma, Inc.)


Welcome to the PulseAid listing for the Armodafinil drug offered from Actavis Pharma, Inc.. This 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: Actavis Pharma, Inc.
NON-PROPRIETARY NAME: Armodafinil
SUBSTANCE NAME: ARMODAFINIL
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: NDA AUTHORIZED GENERIC
START MARKETING DATE: 2016-06-01
END MARKETING DATE: 0000-00-00


Armodafinil HUMAN PRESCRIPTION DRUG Details:

Item DescriptionArmodafinil from Actavis Pharma, Inc.
LABELER NAME: Actavis Pharma, Inc.
DEA SCHEDULE: CIV
ACTIVE STRENGTH: 200(mg/1)
START MARKETING DATE: 2016-06-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0591-3856_cfa0ae8e-1c94-42e8-a19c-7278cc5cf634
PRODUCT NDC: 0591-3856
APPLICATION NUMBER: NDA021875

Other ARMODAFINIL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Actavis Pharma, Inc.Armodafinil
Aurobindo Pharma LimitedArmodafinil
Breckenridge Pharmaceutical, Inc.Armodafinil
Cephalon, Inc.Nuvigil
KAISER FOUNDATION HOSPITALSNuvigil
Lake Erie Medical DBA Quality Care Products LLCArmodafinil
Lupin Pharmaceuticals, Inc.Armodafinil
Mylan Pharmaceuticals Inc.Armodafinil
Rebel Distributors CorpNuvigil
Sandoz Inc.Armodafinil
STAT Rx USA LLCNUVIGIL
Teva Pharmaceuticals USA, Inc.Armodafinil
Watson Laboratories, Inc.Armodafinil