while XXXX quarter revenue delivered welcome to year-over-year year making Building strong and adjusted of footing. have our our started fourth excellence and mentality. the on in those the of We focus another consecutive Thank patient-centered EBITDA. We our both established operational you, momentum, of last we maintaining quarter on this on joining morning. call you and growth growth
of excluding basis. For reported growth or Health, Bausch segments quarter X% an when B&L, the a on growth. quarter prior by organic X% year. delivered were was of basis to the billion, organic first Health, first $XX both XXXX, organic Bausch XXXX, revenue $X.XX for million on on to a All basis compared up Solta revenues and excluding B&L, approximately an led million, and EBITDA compared of $XXX XX% for Adjusted X% with increase reported the
on timing the progress R&D with quarter, our during line make to key our continue initiatives also in established We goals.
First, for a Phase ulcerative colitis, Amiselimod, III meeting we in and of UC. with Phase for met FDA for mild II to end meeting April, planning severe the an
at XXth. a presentation In addition, we pleased were Digestive to accepted for have been Amiselimod Week podium on May for also
completed enrollment first second ahead Second, of Phase which for goal the April, of we III of for completion is slightly global of the end trial our by late RED-C XXXX. half in our
Overall, we of to And the our year. made good we shared we to time have and half anticipate could February. continue for this the and are lines in pursuing occur according of in progressing progress approval third, we pipeline feel second are the CABTREO about the R&D Canada on
the of Circuit court's and the On of Norwich. Federal our order. XX, April judgment U.S. also modification XXXX, August of Turning the for the the had that Norwich affirmed Pharmaceuticals to Delaware's litigation with motion XXXX, Court final May decision Court XXXX, U.S. Appeals for XX, denied XX, District
version patent Amneal XXXX, of On filed the Paragraph that IV notice FDA We until formally FDA we approval a of are the the maintained to the under pharmaceuticals a Xifaxan potential against lawsuit of Circuit receipt XX-month ANDA pleased ANDA XXXX. April an initiates any judgment litigation submitted the preventing the approval of Hatch-Waxman's certification Federal for a the had for ANDA. a Norwich's and of generic Amneal Xifaxan.
This stay Act approval action triggers market X, October Amneal's that stating following seeking process to
in intellectual to property deserves health patients our benefited chance to we to to every As from most the health, are and continue our to the forward the to have gastroenterology for better of vigorously leader make of advocating continued who life. look outcomes a Xifaxan.
We defend committed serve patients as access safety and patient continuing
matter, we in coming the with Trust to On settlement the the months. IRS the be expect continue finalized Granite to
company's As we the have have of material flows. results indicated, previously the impact cash not anticipated the on does or settlement outcome
first on million liquidity we $XXX of bonds sheet focus to billion debt of $X.X approximately continue million our quarter and on of balance as $XXX XXXX the repaid and including our noted maturities over the We with QX, and year-end XXXX ended with call. liquidity.
In
+ separation now The + a priority. Bausch of Turning potential to the Lomb of be Lomb. full strategic full continues to separation Bausch
the regarding strategies evaluate to full separation. continue potential We
be result toward occurs be full other that and at appeals transaction approvals. companies.
The two based to to if relevant on objective subject in all its B&L. assessment a of decision the an and Any of shareholder Norwich structure Any when milestone and will the separation and factors potential will circumstances. a any subject outcome significant of of applicable the also capitalized quarter or represents separation With ensuring matter separation the in appropriately regarding
reported of non-promoted X.
Salix our to X% and of Slide overview growth grew by driven segment Relistor X% Xifaxan with by year-over-year now organic revenue performance Turning offset for for and pressure the quarter, growth on net of pricing and certain slightly an products. starting Trulance
year, in expect demand an see Trulance, and in X%, to TRx grew X% will products Relistor, X%, continued of year. strategy reinforcing tools, our for continuing revenues respectively. to our quarter Overall, we of X% last this DTC primarily further over Xifaxan we investments the important quarter, increase growth first sales make advertising, franchise with growth key this drive which Xifaxan, in of the During AI-enabled
year-over-year Organic growth Canada, quarter. saw X%. Contrave of by organic during led with X% solid We international. revenue quarter and growth first where strong we to growth from performance the of in was saw a growth Turning the reported
on DTC for pleased product foam through we this We XX% Asia this our our in public driving the also growth and promoted XX% long-term build to also investments have ongoing begun organic products on health in efforts. are first Aerosol an revenues focused were UCERIS Pacific. marketing by Canada.
Across investing for in Medical, and to receive increased segment, on business We listing plan led Solta basis, a development reported In by momentum. on
Thermage in with meaningful as growth year-over-year where organic in a we pleased focused the reported delivered believe Asia we solid highly on the China driving business. We quarter there revenue. U.S. medical over growth is prior Diversified, now see Importantly, X% the dermatology return growth to on are This and FLX a and X% to approved in year. was and device posting by momentum remain in markets XX% with EMEA led growth opportunity.
In we U.S. maintaining
late As been early we volume discussed on encouraging. our has U.S. year-end call, January CABTREO and the launched script in in
the capitalize new as over contributor opportunities the to market the significant created supply by constraints. product expect slightly Neurology more competitor continue the we be a to remainder on year. the We grew in to the of revenues dermatology business
higher of investments business challenging expect offset and cash our by on and growth and our in Wellbutrin in we we the to where strategy opportunities declines Aplenzin, managing pressures investments targeted slight pricing generics reinforcing consistent our led script dentistry profitability. competitive generation appropriate. products as profitability our continued focus of on to a net these was volume make a see did where will in we sales XXXX.
Overall, through remainder this mature expected, decline pricing business in continue growth and improved While portfolio lead of while to for for environment looking managing This products to
R&D the GI pipeline. starting developments our in on pipeline Slide X, with latest Turning to our
antagonist and you presentation including XXth gastroenterology As December, for has in evaluating Annual Disease prestigious international on this Japan for our a expect of recall, with EMEA of later Amiselimod II Digestive May are positive selected FDA Amiselimod at the professionals. with we Conference, to a held year. most April authorities, and results UC.
We largest and we Phase In been announced the events podium pleased the that the III in one top meantime, Week's the for meeting treatment Phase study meet and will planning line in from SXP
continue a program move for the II end the by for that with initiate to forward Phase We of planning expect Crohn's to disease year. and
Turning to cirrhosis. with RED-C in early for program our rifaximin reduction decompensation for of
hepatic XXXX. Our global our the underway. deformulation program program Both mentioned, completed Enrollment in efficacy global hospitalizations. previously X,XXX of which as trial, XXXX, trial our rifaximin North and for XXXX, first the of; over across related versus to America, in of focused and half enrollment encephalopathy to this the on Pacific. the expected these SS of Phase first trials December placebo of III occurrence second goal are for assessing delay the include completed the was ahead Asia studies are for for April Europe patients Together,
now pipeline. our to Turning aesthetics
Products and following for an quarter in and could We by return We the to laser in year. National have of half for approval to skin are Thermage file second plan January be in FDA approval TRX Fraxel pad anticipate resurfacing in as this received available QX, second the to submission China the a fractionated the XXXX. Administration of pleased customers next-generation device our the SLX Medical
skin and clear to laser rejuvenation Finally, for advance. brilliant for fractionated our program a touch, continues device
we this New Zealand on products representing our continue and we feel Europe, are Pacific to this products. and the outside new in our United we regulatory the remain durable in first of markets. XXXX about portfolio global year, and progress on good and have of focused authorization submissions on these R&D grow pipeline remain aesthetics as approvals We in received for track other key initiatives, of States Asia making next-generation Australia market approval We and Canada
making committed by assets, leadership investments existing driving team, are and a with leveraging excellence. As targeted commercial we to our growth executing
first to a to continuing mentality.
With will further that, pipeline, details John? call the patient-centered with all performance, over turn the I who John our provide Barresi, on will progress quarter While