8-K

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                                  UNITED STATES
                       SECURITIES AND EXCHANGE COMMISSION

                             WASHINGTON, D.C. 20549


                                    FORM 8-K

                                 CURRENT REPORT
     PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

Date of Report (Date of earliest event reported): June 14, 2005

                          SCHERING-PLOUGH CORPORATION
             (Exact Name of Registrant as Specified in its Charter)


                                                                 
           New Jersey                          1-6571                      22-1918501
(State or Other Jurisdiction of        (Commission File Number)          (IRS Employer
  Incorporation)                                                       Identification Number)




                            2000 Galloping Hill Road
                              Kenilworth, NJ 07033
                     (Address of Principal Executive Office)

       Registrant's telephone number, including area code: (908) 298-4000


Check the appropriate box below if the Form 8-K filing is intended to
simultaneously satisfy the filing obligation of the registrant under any of the
following provisions:


[ ] Written communications pursuant to Rule 425 under the Securities Act (17 CFR
230.425)


[ ] Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR
240.14a-12)


[ ] Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange
Act (17 CFR 240.14d-2(b))


[ ] Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange
Act (17 CFR 240.13e-4(c))

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Item 7.01 Regulation FD Disclosure.

Schering-Plough Corporation from time to time issues Frequently Asked Questions
and Answers (FAQs) that are believed to be of interest to investors. The most
recent FAQs, dated June 14, 2005, are furnished as Exhibit 99.1 to this 8-K and
are posted on the Schering-Plough Website at www.schering-plough.com under
"investor relations/investor publications."

Schering-Plough undertakes no obligation to update the FAQs and readers should
note the date of information when referring to the FAQs or other historical
information available on the website.


Item 9.01 Financial Statements and Exhibits

The following exhibits are furnished with this 8-K:

99.1 June 14, 2005, Investor Frequently Asked Questions and Answers


                                   SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the
registrant has duly caused this report to be signed on its behalf by the
undersigned hereunto duly authorized.


Schering-Plough Corporation


By:  /s/ Douglas J. Gingerella
  ----------------------------
Douglas J. Gingerella
Vice President and Controller

Date:  June 14, 2005

Exhibit Index


The following exhibits are furnished with this 8-K:

99.1 June 14, 2005, Investor Frequently Asked Questions and Answers

EX-99.1

                                                                    EXHIBIT 99.1

      JUNE 14, 2005, INVESTOR FREQUENTLY ASKED QUESTIONS (FAQS) AND ANSWERS

      FROM TIME TO TIME, INVESTOR RELATIONS WILL PROVIDE FAQS AND ANSWERS ON
      VARIOUS TOPICS OF INTEREST TO INVESTORS. THE FOLLOWING IS A COMPILATION OF
      RECENT FAQS AND ANSWERS.


Q     WHAT IS THE STATUS OF YOUR CCR5 INHIBITOR FOR HIV?

A     The U.S. Food and Drug Administration (FDA) recently granted Fast Track
      designation to Schering-Plough's CCR5 receptor antagonist vicriviroc for
      the treatment of HIV infection. FDA Fast Track programs are designed to
      facilitate the development and expedite the review of new drugs that are
      intended to treat serious or life-threatening conditions and that
      demonstrate the potential to address unmet medical needs.

      Vicriviroc is currently being studied in two Phase II clinical trials, one
      in the United States and one in Europe and Canada. The company expects to
      begin Phase III clinical studies with vicriviroc this summer.


Q     WHAT IS THE STATUS OF POSACONAZOLE AT THE FDA? EUROPE?

A     Schering-Plough received an approvable letter from the U.S. FDA on June
      10, 2005 for its New Drug Application (NDA) for posaconazole, an oral
      antifungal agent. The company is assessing the FDA's request for
      additional data and will respond to the FDA as soon as possible in order
      to continue the U.S. regulatory review for this new treatment for patients
      with serious fungal infections. Posaconazole is currently under regulatory
      review in Europe.


Q     HOW IS THE LAUNCH OF PEG-INTRON/REBETOL IN JAPAN PROGRESSING?

A     Schering-Plough is pleased with the early launch success of PEG-INTRON in
      Japan.

      Since its December launch, PEG-INTRON in combination with REBETOL has
      become the leading Hepatitis C treatment in Japan and already holds over
      40 percent market share, according to IMS data. On a combined basis,
      PEG-INTRON and INTRON A have more than 50 percent market share in Japan,
      according to IMS data.

      For the remainder of 2005, we anticipate continued sales growth of
      PEG-INTRON in Japan, on a year-over-year basis. Sales in Japan are
      benefiting from the significant number of patients who were waiting for
      approval of PEG-INTRON before beginning treatment ("patient warehousing").
      Comparisons in 2006 will be unfavorably impacted by the absence of this
      patient warehousing.

      It is estimated that between 1.5 million and 2 million people in Japan are
      infected with Hepatitis C. Hepatitis C is the leading cause in Japan of
      chronic liver disease,




      cirrhosis, and hepatocellular carcinoma, which is associated with more
      than 30,000 deaths there annually.

Q     DO YOU HAVE INVENTORY MANAGEMENT AGREEMENTS (IMAS) WITH U.S.
      PHARMACEUTICAL WHOLESALERS FOR ZETIA AND VYTORIN?

A     Recently, Merck Schering-Plough Cholesterol Partnership entered
      into inventory management agreements with the major U.S.
      pharmaceutical wholesalers.

      Schering-Plough also has existing inventory management agreements in place
      for its other products.

Q     IN WHICH EUROPEAN COUNTRIES HAVE YOU LAUNCHED VYTORIN/INEGY AND
      ZETIA/EZETROL?

A     EZETROL has been launched in many European countries, including Germany,
      France, Spain, United Kingdom, Ireland, Sweden, and Switzerland.

      Currently, INEGY has been launched in Germany, The Netherlands, Ireland,
      and Portugal. The launch in the United Kingdom has recently been
      initiated.


Q     HOW WOULD YOU CHARACTERIZE THE ALLERGY SEASON IN THE U.S. AND
      EUROPE?

A     The allergy season in the U.S. and Europe would best be
      characterized as moderate in the U.S. and Europe, while the season
      in Japan was exceptionally severe for patients with allergies.


      DISCLOSURE NOTICE: This Investor FAQ contains "forward-looking statements"
      within the meaning of the Securities Litigation Reform Act of 1995,
      including statements concerning Vicriviroc and the potential of
      PEG-INTRON in Japan. Forward-looking statements relate to expectations or
      forecasts of future events and not to historical information.
      Schering-Plough does not assume the obligation to update any
      forward-looking statement. Any and all forward-looking statements here or
      in other publications may turn out to be wrong. Actual results may vary
      materially and there are no guarantees about Schering-Plough's financial
      and operational performance or the performance of Schering-Plough stock.
      A number of risks and uncertainties could cause actual results to differ
      from forward-looking statements made here or in other Schering-Plough
      written or spoken communications, including the market viability of the
      company's (and the cholesterol joint venture's) marketed and pipeline
      products; possible changes in business strategies and the ability to
      successfully implement those business strategies; general market and
      economic factors; regulations and legislation; label/use changes or
      concern of prescribers or patients relating to Schering-Plough products,
      other company's products or pharmaceutical products generally; existing
      and new manufacturing issues that may arise; trade buying patterns;
      patent positions; litigation and investigations; and instability or
      destruction in a geographic area important to the company. For a more
      detailed discussion of these and other risks and uncertainties that may
      impact forward-looking statements, see Schering-Plough's Securities and
      Exchange Commission filings, including the 2005 First Quarter 10-Q.