FORM 10-Q/A SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 __________________________________ (Mark One) ----- / X / QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE - - ---- SECURITIES EXCHANGE ACT OF 1934 For the Period Ended December 31, 1995 ----- / / TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE - - ----- SECURITIES EXCHANGE ACT OF 1934 For the transition period from __________ to ________________________________ Commission File No. 1-5438 FOREST LABORATORIES, INC. - - ---------------------------------------------------------------------------- (Exact name of registrant as specified in its charter) Delaware 11-1798614 - - ------------------------------- --------------------- (State or other jurisdiction of (I.R.S. Employer incorporation or organization) Identification No.) 909 Third Avenue - - ---------------- New York, New York 10022-4731 - - -------------------- ------------------- (address of principal (Zip Code) executive office) Registrant's telephone number, including area code 212-421-7850 ------------------- Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15 (d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes X No ----- ----- Number of shares outstanding of Registrant's Common Stock as of February 14, 1996: 45,425,940. PAGE FOREST LABORATORIES, INC. AND SUBSIDIARIES Item 2. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS FINANCIAL CONDITION AND LIQUIDITY The financial condition of the Company - - --------------------------------- continues to be strong. The decrease in cash, marketable securities and long-term marketable securities as well as the increase in intangible assets and investments in subsidiaries, net was principally the result of the acquisition of a minority interest in the common stock of Biovail Corporation International which was done in connection with the acquisition of an exclusive license for the product Tiazac-TM-, a once daily calcium channel blocker and the acquisition of certain product rights from Berlex Laboratories for Climara-R-. The increase in accounts receivable, inventories, accounts payable and accrued expenses were due to the continued growth of the Company's principal promoted products and an increase in the Company's overall level of operations. Company operations have historically provided a strong positive cash flow and management believes that on going operations, when combined with the Company's strong cash position, will continue to provide adequate liquidity to facilitate potential acquisitions of products or companies and other capital investments. RESULTS OF OPERATIONS Net sales for the three and nine month periods ended - - --------------------- December 31, 1995 increased $15,590,000 and $43,888,000 respectively, as compared with the same periods last year. This was primarily due to the continued growth of the Company's principal promoted products, the launch of Cervidil-TM- , the Company's prostaglandin E2 insert used to ripen the cervix in in induced childbirth and Tiazac. Tiazac is a once-daily formulation of diltiazem, a calcium channel blocker used in the treatment of hypertension. Tiazac is marketed as a branded pharmaceutical product and detailed by the Company's sales representatives. Net volume growth of those products amounted to $13,516,000 for the quarter and $46,151,000 for the nine months. Net volume growth of the Company's older unpromoted products amounted to $1,624,000 for the quarter but declined $4,888,000 for the nine months. The remainder of the net sales change was primarily due to price and foreign exchange fluctuations. In November 1993, a patent infringement lawsuit was commenced by Marion Merrel Dow, Inc. ("MMD") and certain related parties against Hoechst-Roussel Pharmaceuticals, Inc. a previous licensee of Biovail Corporation International (BCI") for the Tiazac product. The complaint alleged that Hoechst-Roussel infringed certain patents relating to controlled release diltiazem formulations. In March 1995, Hoechst-Roussel's parent, Hoechst AG, announced its intention to acquire MMD, which acquisition was subsequently consummated. As a result of agreements entered into in connection with such acquisition, Hoechst-Roussel returned all rights to Tiazac to BCI and entered into a settlement and release pursuant to which the patent litigation was dismissed with prejudice. The Company does not believe that there is any basis for any similar patent infringement claim which could be asserted by any third party. Cost of sales as a percentage of sales increased to 21% during the three month period and 20% during the nine-month period from 19% for the same periods last year due mostly to increases in overhead costs related to the Company's facilities expansion and lower net prices received on certain generic products. Selling, general and administrative expenses of the current quarter and nine month periods increased over the same periods last year due primarily to costs incurred in connection with the launch of Cervidil and Tiazac, which included a substantial increase in the sales force, and to support co-promotion agreements previously entered into by the Company. It is anticipated that such increases will continue into the 1997 fiscal year. Research and development expense increased during the current quarter and nine month periods over the same periods last year principally as a result of the cost of conducting clinical trials in order to obtain approval of new products and the cost of developing products using the Company's controlled release technology. During the current quarter and nine month period, there was particular emphasis on Methoxatone, AF102B and Synapton-TM-. Methoxatone is being developed for the treatment of brain trauma and AF102B is an M1 agonist for the treatment of Alzheimer's Disease. Synapton is the Company's controlled release formulation of physostigmine being tested for the treatment of Alzheimer's Disease. -2- 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 thereunto duly authorized. Date: April 22, 1996 Forest Laboratories, Inc. -------------------------- (Registrant) /s/ Howard Solomon ---------------------------- Howard Solomon President and Chief Executive Officer /s/ Kenneth E. Goodman ----------------------------- Kenneth E. Goodman Vice President - Finance -3-