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ULTRAVATE

NDA · New Drug Application · Sponsor: SUN PHARM INDS INC · Approved 1990-12-17

Drug application

FDA Application #

NDA019968

Application type

New Drug Application

Brand name

ULTRAVATE

Generic name

Halobetasol Propionate

Active ingredients

HALOBETASOL PROPIONATE

Dosage form

OINTMENT

Route

TOPICAL

Marketing status

Discontinued

Sponsor

SUN PHARM INDS INC

First approval

1990-12-17

Source

Authoritative

Drugs@FDA application overview

Machine

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