Naratriptan (Sandoz Inc)


Welcome to the PulseAid listing for the Naratriptan drug offered from Sandoz Inc. This Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d 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: Sandoz Inc
NON-PROPRIETARY NAME: Naratriptan
SUBSTANCE NAME: NARATRIPTAN HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
ROUTE: ORAL
DOSAGE FORM: TABLET, COATED
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2010-07-07
END MARKETING DATE: 0000-00-00


Naratriptan HUMAN PRESCRIPTION DRUG Details:

Item DescriptionNaratriptan from Sandoz Inc
LABELER NAME: Sandoz Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 1(mg/1)
START MARKETING DATE: 2010-07-07
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0781-5526_4dda1b06-d3c1-44f4-afb1-b0e31db9e497
PRODUCT NDC: 0781-5526
APPLICATION NUMBER: ANDA090288

Other NARATRIPTAN HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
GlaxoSmithKline LLCAMERGE
Heritage Pharmaceuticals Inc.Naratriptan
OrchidPharma, IncNaratriptan
Paddock Laboratories, LLCNaratriptan Hydrochloride
Sandoz IncNaratriptan
Sun Pharmaceutical Industries LimitedNaratriptan
West-Ward Pharmaceuticals Corp.Naratriptan