Prednicarbate

Dermatop

0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** ointmentUnited StatesNot marketedAuthorised 23 Sept 1991

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In other countries

The same active substances on other registers, the same brand first.

DermatopBrazil · Sanofi Medley Farmacêutica Ltda.Same brand
DermatopBrazil · Sanofi-Aventis Farmacêutica LtdaSame brand
Dermatop Emollient CreamCanada · 0.1 % / W/W · Cream · Bausch Health, Canada INC.Same brand
Dermatop OintmentCanada · 0.1 % / W/W · Ointment · Bausch Health, Canada INC.Same brand
Batmen 2,5 MG/G CremaSpain · 0,250 g · crema · A. Menarini Latin America S.L.Same form
Batmen 2,5 MG/G PomadaSpain · 0,250 g · pomada · A. Menarini Latin America S.L.Same form
Batmen 2,5 MG/G UngüentoSpain · 0,250 g · pomada · A. Menarini Latin America S.L.Same form

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Prednicarbate

Dermatop

0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** ointmentUnited StatesNot marketedAuthorised 23 Sept 1991

Open in the registerAsk Osler about it

In other countries

The same active substances on other registers, the same brand first.

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

Discover Osler

Packs

Pack	Code	Status
PREDNICARBATE 0.1% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	NDA019568-001	Discontinued

Documents

The official texts, at the regulator.

Register entryFDA

Sources and licences

Compiled by Prognia from the public register below; the register’s text is the official one.

U.S. Food and Drug Administration (Drugs@FDA) and openFDA drug labels

Source: U.S. Food and Drug Administration, Drugs@FDA and openFDA drug labels (imported 10 June 2026). Not endorsed by the FDA.

Licence: Public domain (U.S. Government work); openFDA terms · Added 10 Jun 2026

Report an error or request removalCorrections from the holder or the register are welcome.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Active substance: Prednicarbate
Strength: 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form: ointment
Route: topical
Register: United States (FDA)
Status: Not marketed
Status in the register: Discontinued
Authorised: 23 Sept 1991
Registration: NDA 19568
Marketing authorisation holder: Valeant Pharms North
Procedure: NDA

PrednicarbatePrednicarbate · 0.1% · creamUnited States