donidalorsen

FDA Drug Profile — DAWNZERA

donidalorsen is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including DAWNZERA. Available dosage form: injection, solution.

Drug Details

Generic Name
donidalorsen
Brand Names
DAWNZERA
Application Number
NDA219407
Sponsor
Ionis Pharmaceuticals Inc.
NDC Codes
1
Dosage Forms
INJECTION, SOLUTION
Routes
SUBCUTANEOUS
Active Ingredients
DONIDALORSEN SODIUM

Indications and Usage

1 INDICATIONS AND USAGE DAWNZERA™ is indicated for prophylaxis to prevent attacks of hereditary angioedema (HAE) in adult and pediatric patients 12 years of age and older. DAWNZERA is a prekallikrein directed antisense oligonucleotide indicated for prophylaxis to prevent attacks of hereditary angioedema (HAE) in adult and pediatric patients 12 years of age and older. ( 1 )