← FDA Drug Approvals (Drugs@FDA)

METHYLDOPATE HYDROCHLORIDE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: ABRAXIS PHARM · Approved 1986-06-03

Drug application

FDA Application #
ANDA070652
Application type
Abbreviated New Drug Application (Generic)
Brand name
METHYLDOPATE HYDROCHLORIDE
Generic name
Methyldopate Hydrochloride
Active ingredients
METHYLDOPATE HYDROCHLORIDE
Dosage form
INJECTABLE
Route
INJECTION
Marketing status
Discontinued
Sponsor
ABRAXIS PHARM
First approval
1986-06-03

Source

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