Naratriptan (Sun Pharmaceutical Industries Limited)


Welcome to the PulseAid listing for the Naratriptan drug offered from Sun Pharmaceutical Industries Limited. 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: Sun Pharmaceutical Industries Limited
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, FILM COATED
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2011-02-22
END MARKETING DATE: 2017-11-30


Naratriptan HUMAN PRESCRIPTION DRUG Details:

Item DescriptionNaratriptan from Sun Pharmaceutical Industries Limited
LABELER NAME: Sun Pharmaceutical Industries Limited
DEA SCHEDULE:
ACTIVE STRENGTH: 2.5(mg/1)
START MARKETING DATE: 2011-02-22
END MARKETING DATE: 2017-11-30
PRODUCT ID: 62756-437_cca227e8-db14-41bb-9eb1-62a19f26a0f1
PRODUCT NDC: 62756-437
APPLICATION NUMBER: ANDA091552

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