8-K

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): September 26, 2014

Eagle Pharmaceuticals, Inc.

(Exact name of registrant as specified in its charter)

Delaware	001-36306	20-8179278
(State or other jurisdiction	(Commission File Number)	(IRS Employer Identification No.)
of incorporation)

50 Tice Boulevard, Suite 315 Woodcliff Lake, NJ	07677
(Address of principal executive offices)	(Zip Code)

Registrant’s telephone number, including area code: (201) 326-5300

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

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

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

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

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

Item 8.01Other Events

On September 26, 2014, Eagle Pharmaceuticals, Inc., or the Company, will present the attached discussion of the Company’s business model, products and product candidates at BioCentury’s 21st Annual NewsMakers in the Biotech Industry Conference, being held at the Millennium Broadway Hotel & Conference Center in New York City.

A copy of the above referenced presentation is filed as Exhibit 99.1 to this Current Report on Form 8-K.

Item 9.01Financial Statements and Exhibits.

(d)Exhibits

Exhibit No.	Description
99.1	Presentation of the Company dated September 26, 2014

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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.

	Eagle Pharmaceuticals, Inc.
Dated: September 26, 2014
	By:	/s/ Scott Tarriff
		Scott Tarriff
		President and Chief Executive Officer

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EXHIBIT INDEX

Exhibit No.	Description
99.1	Presentation of the Company dated September 26, 2014

4

EX-99.1

Exhibit 99.1

September 2014 Scott Tarriff, CEO David Riggs, CFO NASDAQ: EGRX

 Forward Looking Statements 2 This presentation contains certain forward-looking information about Eagle Pharmaceuticals that is intended to be covered by the safe harbor for "forward-looking statements" provided by the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts. Words such as “anticipate,” “believe,” “estimate,” “expect,” “intend,” “may,” “plan,” “predict,” “project,” “target,” “potential,” “will,” “would,” “could,” “should,” “continue,” “strong,” “up coming,” and similar expressions are intended to identify forward-looking statements. These statements include, but are not limited to, statements regarding our ability to successfully develop and commercialize our therapeutic products; our ability to expand our long-term business opportunities; financial projections and estimates and their underlying assumptions; and future performance. All such statements are subject to certain risks and uncertainties, many of which are difficult to predict and generally beyond the Company’s control, that could cause actual results to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include, but are not limited to: whether our product candidates will be successfully marketed and obtain commercial success after regulatory approval; whether any of our product candidates will advance further in the clinical trials process and whether and when, if at all, they will receive final approval from the U.S. Food and Drug Administration or equivalent foreign regulatory agencies and for which indications; whether our discovery and development efforts relating to improved formulations and delivery methods for existing FDA-approved products will be successful and/or our ability to select and acquire or in-license product candidates; our ability to achieve the results contemplated by our collaboration arrangements; the strength and enforceability of our intellectual property rights; competition from biotechnology and pharmaceutical companies; our ability to raise additional capital to fund our operations on terms acceptable to us; general economic conditions; and the other risk factors included in our final prospectus filed with the Securities and Exchange Commission on February 13, 2014 relating to our Registration Statement on Form S-1 (File No. 333-192984) for our IPO and other periodic an interim reports filed from time to time with the SEC. Our audience is cautioned not to place undue reliance on these forward-looking statements that speak only as of the date hereof, and we do not undertake any obligation to revise and disseminate forward-looking statements to reflect events or circumstances after the date hereof, or to reflect the occurrence of or non-occurrence of any events.

Eagle Pharmaceuticals Nasdaq: EGRX Specialty pharmaceutical company Differentiated forms of branded injectables Validated strategy Near-term Commercial Opportunities Bendamustine RTD Tentative Approval July 2, 2014 Ryanodex approved July 22 & launched August 2014 Diclofenac/misoprostol approved March 2014 Long life cycles = significant value Strong IP around differentiating features Orphan drug designations Well capitalized to execute Cash as of June 30, 2014 $49.8 million

Validated Business Model In-market product: Argatroban Improved formulation of branded drug Ready-to-use; no dilution Significant reduction in drug waste Entered market three years before first generic Our partners net sales & margins over last 12 months 1 Source: IMS Net Sales $ 24.6M COGS 4.9 Gross Profit $ 19.7M 79% margin

Late Stage Portfolio Targeting Proven Markets Bendamustine RTD Bendamustine RTD Low-volume, shorter infusion time Ryanodex (dantrolene): Malignant Hyperthermia Ryanodex: Exertional Heat Stroke RTU bivalirudin Pemetrexed Argatroban Tentative Approval 7/2/14 Launched 8/29/14 1 Source: publicly filed reports with the SEC, independent market research and management’s estimates

Bendamustine RTD Improved formulation of Treanda1 for CLL2 & NHL3 Ready-to-dilute concentrated liquid of cytotoxic API Same volume diluent, same infusion time 7/2/14 received tentative approval for NHL Commercial launch Window - 2015 through early 2016 Longevity post-launch: 1 issued patent & 4 filed Expiry expected 2031-33 Patent litigation – ahead of ANDA litigation Plaintiff filed Motion to dismiss ‘524 infringement case Teva initiated new ‘270 infringement case in August 1 Treanda® (bendamustine HCl) (Cephalon, Inc., a wholly-owned subsidiary of Teva Pharmaceutical Industries Ltd.) 2 CLL: chronic lymphocytic leukemia 3 NHL: indolent B-cell non-Hodgkin lymphoma

Lower-volume Shorter Infusion Time Bendamustine RTD Highlights Patient Benefit Less chair time: 30 or 60 minutes reduced to 10 minutes Less volume and the issues related to 50ml vs. 500mL Longer Shelf Life (less degradation products) Eliminates the need for exposure to DMA Nurse Less nursing time required Medical/Patient 90% reduction in NaCl – renal suppressed population Economic Benefit Additional patients treated in the cancer clinic due to shorter infusion time Anticipated to sell for slightly less than innovator

Lower-volume Shorter Infusion Time Bendamustine RTD Same product as bendamustine RTD Dilute in 50mL admixture rather than in 500mL Potential to convert market based on improved product attributes Received Orphan drug designation for CLL and NHL July 2, 2014 May afford 7 years exclusivity on approval Depomed Gralise Court Decision One issued patent with expiration date in June 2031

Lower-volume Shorter Infusion Time Bendamustine RTD Randomized, blinded clinical trial Phase I PK/Safety Study Enrollment complete, data results anticipated by year-end

No change to SOC for MH treatment in over 30 years Can be fatal if untreated Old product typically requires 720 ml (12 vials) Eagle optimized formulation reduces to 5ml (1 vial) Breakthrough change Expected to take over market Launched Ryanodex 8/29/14 Protected market position 3 patents issued + 1 filed Orphan drug designation for MH EU regulatory submission expected to be filed by 2015 Ryanodex (dantrolene) for Malignant Hyperthermia (MH) 1 Retrospective study conducted by the Malignant Hyperthermia Association of the United States (MHAUS)

Ryanodex US Commercial Landscape Branded dantrolene sales for MH ~$20M in 2013 Ryanodex pricing expands addressable market Ryanodex advantages support premium pricing Faster administration Reduced volume Significant reduction of Mannitol (diuretic) All 6,000 US hospitals required to stock dantrolene MHAUS1 recommends a minimum of 36 vials of old product vs. 3 vials of Ryanodex Market unlikely to revert to old 720ml formulation Eagle is commercializing (without partnering) Established small contract sales Commercial infrastructure in-place 1 MHAUS: Malignant Hyperthermia Association of the United States

Why Dantrolene? MH Exertional Heat Stroke Ecstasy Overdose Duchenne Europe ROW Initial indication: Malignant Hyperthermia Larger markets + Unmet needs Further opportunity for all indications Malignant Hyperthermia is just the tip of the iceberg Rhabdomyolysis

Ryanodex Label Expansion Opportunity Exertional Heat Stroke (EHS) Est. 23,000-38,000 cases/year1 A leading cause of student athlete death (US) & non-combat military deaths Similarities to MH Potential for Ryanodex to be first to market for EHS Orphan drug designation for EHS Potential for 7-10 year life cycle w/o competition Market estimated at $150M 1 Estimate based on 2010 population projections

Bivalirudin: $550M – Approximate Brand Sales Enhanced RTU version of the anticoagulant Angiomax Completed three registration batches for NDA submission 2 patents issued; third patent filed 1Q:14 NDA submission targeted for Q2:15 US launch planned as early as Q1:16

Pemetrexed: $1.21B Opportunity Liquid version of Alimta, a powder cytotoxic API No reconstitution & dilution Less exposure to cytotoxic vapors for healthcare staff Expect to launch with generics (2017-21)

US Patents Longevity Orphan Drug FDA Action Issued Filed Argatroban 2 1 Sept 2027 In-market Bendamustine RTD: NHL & CLL 1 4 Jan 2031- Mar 2033 Yes Tentative Approval 7/2/14 Ryanodex (dantrolene): MH 3 1 Jul 2022- Jul 2025 Yes In-market Ryanodex: Heat stroke/EHS 1 Feb 2023 Yes RTU bivalirudin 21 1 Aug 2029- May 2034 Other 2 3 Feb 2027– Dec 2032 TOTAL 11 10 3 Combination Approach for Long Life Cycle 1 Jointly owned by Medicines Co. & Eagle Patents expected to be Orange Book listed & potentially result in 30 month stays + potential long term protection

Investment Considerations Over $3.4 billion opportunity in injectable products space Recent Bendamustine tentative approval and Ryanodex approval Near term product launch opportunities with high margins 3 Orphan Drugs: Ryanodex EHS & MH and bendamustine LV Strong IP portfolio to protect market position: 11 patents issued Long life cycle creates significant value opportunity Strong balance sheet with over $49.8M in cash1 1 As of the quarter ended June 30, 2014

September 2014