Naratriptan Hydrochloride (Paddock Laboratories, LLC)


Welcome to the PulseAid listing for the Naratriptan Hydrochloride drug offered from Paddock Laboratories, LLC. 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: Paddock Laboratories, LLC
NON-PROPRIETARY NAME: Naratriptan Hydrochloride
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: 2010-07-08
END MARKETING DATE: 0000-00-00


Naratriptan Hydrochloride HUMAN PRESCRIPTION DRUG Details:

Item DescriptionNaratriptan Hydrochloride from Paddock Laboratories, LLC
LABELER NAME: Paddock Laboratories, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 1(mg/1)
START MARKETING DATE: 2010-07-08
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0574-0214_ff4c0d67-2618-4bd5-a8e2-9c2dbab0a710
PRODUCT NDC: 0574-0214
APPLICATION NUMBER: ANDA091326

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