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METHYLDOPATE HYDROCHLORIDE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: AM REGENT · Approved 1987-12-02

Drug application

FDA Application #
ANDA071279
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
AM REGENT
First approval
1987-12-02

Source

Authoritative
Drugs@FDA application overview
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