PALTUSOTINE

FDA Drug Profile — PALSONIFY

PALTUSOTINE is listed in the FDA National Drug Code directory with 2 NDC codes, marketed under brand name including PALSONIFY. Available dosage form: tablet, film coated.

Drug Details

Generic Name
PALTUSOTINE
Brand Names
PALSONIFY
Application Number
NDA219070
Sponsor
Crinetics Pharmaceuticals, Inc.
NDC Codes
2
Dosage Forms
TABLET, FILM COATED
Routes
ORAL
Active Ingredients
PALTUSOTINE HYDROCHLORIDE

Indications and Usage

1 INDICATIONS AND USAGE PALSONIFY is indicated for the treatment of adults with acromegaly who had an inadequate response to surgery and/or for whom surgery is not an option. PALSONIFY is a somatostatin receptor agonist indicated for the treatment of adults with acromegaly who had an inadequate response to surgery and/or for whom surgery is not an option ( 1 ).