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MINOCIN

NDA · New Drug Application · Sponsor: REMPEX · Approved 1972-10-26

Drug application

FDA Application #
NDA050444
Application type
New Drug Application
Brand name
MINOCIN
Generic name
MINOCYCLINE HYDROCHLORIDE
Active ingredients
MINOCYCLINE HYDROCHLORIDE
Dosage form
INJECTABLE
Route
INJECTION
Marketing status
Prescription
Sponsor
REMPEX
Manufacturer
Melinta Therapeutics, LLC
First approval
1972-10-26

Source

Authoritative
Drugs@FDA application overview
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