Naratriptan

Product NDC

0781-5527

11-digit product format

007815527

Labeler code

0781

Product ID

0781-5527_49acb238-7bf5-4f86-925f-c939b4ece684

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Naratriptan

Dosage form

TABLET, COATED

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA090288

Marketing category

ANDA

Marketing start

2010-07-07

Marketing end

2019-11-08

Substance

NARATRIPTAN HYDROCHLORIDE

Active strength

3 mg/1

Pharmacologic classes

Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record