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Last $306.10 USD
Change Today -1.91 / -0.62%
Volume 644.7K
As of 11:37 AM 08/31/15 All times are local (Market data is delayed by at least 15 minutes).

allergan plc (AGN) Snapshot

Open
$310.85
Previous Close
$308.01
Day High
$312.64
Day Low
$305.02
52 Week High
07/29/15 - $340.34
52 Week Low
10/15/14 - $208.64
Market Cap
120.3B
Average Volume 10 Days
2.8M
EPS TTM
$1.52
Shares Outstanding
393.6M
EX-Date
--
P/E TM
200.6x
Dividend
--
Dividend Yield
--
Current Stock Chart for ALLERGAN PLC (AGN)

allergan plc (AGN) Details

Allergan plc develops, manufactures, and distributes generic, branded, biosimilar, and over-the-counter (OTC) pharmaceutical products. It operates in three segments: North American Brands, North American Generics and International, and Anda Distribution. The North American Brands segment provides patented and off-patent trademarked pharmaceutical products primarily under the Dalvance, Bystolic, Canasa, Carafate, Daliresp, Fetzima, Linzess, Namenda, Namenda XR, Saphris, Teflaro, Viibryd, Actonel, Asacol HD, Atelvia, Delzicol, Doryx, Estrace Cream, Enablex, Lo Loestrin Fe, and Minastrin 24 Fe brands. The North American Generics and International segment develops, manufactures, and sells generic, branded generic, and OTC pharmaceutical products. The Anda Distribution segment distributes generic and brand pharmaceutical products primarily to independent pharmacies, pharmacy chains and buying groups, and physician’s offices. The company also develops and out-licenses generic pharmaceutical products primarily in Europe through its third-party business; and provides products in women's health, gastroenterology, urology, and dermatology areas. The company sells its generic and brand pharmaceutical products primarily to drug wholesalers, retailers, and distributors, including national retail drug and food store chains, hospitals, clinics, mail order retailers, government agencies, and managed healthcare providers. It has a collaboration agreements with Amgen, Inc. to develop and commercialize biosimilar versions of Herceptin, Avastin, Rituxan/Mab Thera, and Erbitux; Ironwood Pharmaceuticals to develop and commercialize Linzessfor the treatment of irritable bowel syndrome with constipation and chronic idiopathic constipation; Sanofi-Aventis U.S. LLC; and Trevena for the development of TRV027. The company was formerly known as Actavis plc and changed its name to Allergan plc in June 2015. Allergan plc was founded in 1983 and is headquartered in Parsippany, New Jersey.

21,600 Employees
Last Reported Date: 02/18/15
Founded in 1983

allergan plc (AGN) Top Compensated Officers

Chief Executive Officer, President and Direct...
Total Annual Compensation: $500.0K
Executive Chairman
Total Annual Compensation: $1.0M
Chief Financial Officer and Executive Vice Pr...
Total Annual Compensation: $31.4K
Executive Vice President and President of Gen...
Total Annual Compensation: $707.5K
Executive Vice President and President of Bra...
Total Annual Compensation: $272.5K
Compensation as of Fiscal Year 2014.

allergan plc (AGN) Key Developments

Allergan plc Recalls in the U.S. of Specific Lots of REFRESH Lacri-Lube, REFRESH P.M., FML (Fluorometholone Ophthalmic Ointment) 0.1%, and Blephamide(Sulfacetamide Sodium and Prednisolone Acetate Ophthalmic Ointment, USP) 10%/0.2% for Particulate Matter

Allergan plc announced that it is conducting a voluntary recall down to consumer level of specific lots of its REFRESH Lacri-Lube 3.5g and 7g for dry eye, REFRESH P.M. 3.5g for dry eye, FML (fluorometholone ophthalmic ointment) 0.1% (sterile ophthalmic ointment topical anti-inflammatory agent for ophthalmic use, 3.5g), and Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10%/0.2% sterile topical ophthalmic ointment combining an antibacterial and a corticosteroid, 3.5g. The company chose to initiate this recall based on a small number of customer complaints which reported a small black particle at the time of use. This black particle, which is part of the cap, can be created by the action from unscrewing the cap of the aluminum tube, and potentially introduced into the product. Reported adverse events include Foreign Body in Eye (12), Eye Irritation (2), Ocular Discomfort (2), Product Contamination (2), Superficial Injury of Eye (2), Eye Pain (1), Eye Swelling (1) and Vision Blurred (1). The company has informed the U.S. Food and Drug Administration of this voluntary recall. The recall only applies to specific lots of the REFRESH Lacri-Lube, REFRESH P.M., FML (fluorometholone ophthalmic ointment) 0.1%, Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10%/0.2%. This recall does not affect any other REFRESH or Allergan product.

U.S. Food and Drug Administration Accepts Allergan plc's BOTOX (onabotulinumtoxinA) Resubmission for the Treatment of Lower Limb Spasticity in Adults

Allergan plc announced that the U.S. Food and Drug Administration (FDA) has accepted the company's resubmission of its Supplemental Biologics License Application (sBLA) for BOTOX (onabotulinumtoxinA) for the treatment of adults with lower limb (involving ankle and toe muscles) spasticity in adults. A six-month review period has been assigned for the sBLA. The Prescription Drug User Fee Act (PDUFA) date is expected to be in the first quarter of 2016. The resubmission provides additional data from a double-blind, placebo controlled study involving 468 patients with lower limb spasticity. In April 2015, the FDA approved an expansion of the BOTOX (onabotulinumtoxinA) label for the treatment of adults with upper limb spasticity. The expanded label now includes the addition of two thumb muscles: flexor pollicis longus, a muscle in the forearm that flexes the thumb; and adductor pollicis, a muscle in the hand that functions to adduct the thumb; increasing the maximum dose from 360 to 400 units for the treatment of upper limb spasticity. The FDA also approved an increase to the maximum BOTOX cumulative dose within three months from 360 to 400 units in adults treated for one or more indications.

Allergan Files ANDA with FDA Seeking Approval to Market Posaconazole Delayed-Release Tablets, 100Mg; Merck Sharp & Dohme Corp. Files Suit Against Allergan Seeking to Prevent Allergan from Commercializing its Anda Product Prior to the Expiration of U.S. Patent No. 5,661,151

Allergan plc confirmed that it has filed an Abbreviated New Drug Application (ANDA) with the U.S. Food and Drug Administration (FDA) seeking approval to market Posaconazole Delayed-Release Tablets, 100mg. Allergan's ANDA product is a generic version of Merck's Noxafil which is an antifungal agent indicated for prophylaxis of invasive Aspergillus and Candida infections in patients, 13 years of age and older, who are at high-risk of developing these infections due to being severely immunocompromised, such as hematopoietic stem cell transplantation recipients with graft-versus-host disease or those with hematologic malignancies with prolonged neutropenia from chemotherapy. Merck Sharp & Dohme Corp. filed suit against Allergan on August 6, 2015 in the U.S. District Court for the District of New Jersey seeking to prevent Allergan from commercializing its ANDA product prior to the expiration of U.S. Patent No. 5,661,151. The lawsuit was filed under the provisions of the Hatch-Waxman Act, resulting in a stay of final FDA approval of Allergan's ANDA for up to 30 months from the date the plaintiffs received notice of Allergan's ANDA filing or until final resolution of the matter before the court, whichever occurs sooner, subject to any other exclusivities.

 

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Industry Analysis

AGN

Industry Average

Valuation AGN Industry Range
Price/Earnings NM Not Meaningful
Price/Sales 6.8x
Price/Book 1.8x
Price/Cash Flow 66.7x
TEV/Sales 4.1x
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