← FDA Drug Approvals (Drugs@FDA)

ULTIVA

NDA · New Drug Application · Sponsor: MYLAN INSTITUTIONAL · Approved 1996-07-12

Drug application

FDA Application #
NDA020630
Application type
New Drug Application
Brand name
ULTIVA
Generic name
REMIFENTANIL HYDROCHLORIDE
Active ingredients
REMIFENTANIL HYDROCHLORIDE
Dosage form
INJECTABLE
Route
INJECTION
Marketing status
Prescription
Sponsor
MYLAN INSTITUTIONAL
Manufacturer
Mylan Institutional LLC
First approval
1996-07-12

Source

Authoritative
Drugs@FDA application overview
Machine
JSON-LD · Markdown