AMAG Pharmaceuticals
1100 Winter Street
Waltham
Massachusetts
02451
United States
Tel: 617-498–3300
Fax: 617-499-3361
Website: http://www.amagpharma.com/
Email: contactus@amagpharma.com
About AMAG Pharmaceuticals
Founded in 1981, AMAG Pharmaceuticals is committed to improving the health outcomes of patients through the development and commercialization of specialty pharmaceutical products.
AMAG currently markets a therapeutic intravenous iron compound for the treatment of iron deficiency anemia in adult patients with chronic kidney disease (CKD) and an oral rinse for the management of oral mucositis in the United States. To learn more about our products, click here. Along with driving organic growth of its lead product, AMAG intends to expand its portfolio with additional commercial-stage specialty pharmaceuticals. The company is seeking complementary products that leverage the company's commercial footprint and focus on hematology and oncology centers and hospital infusion centers.
Our iron oxide particles are composed of bioavailable iron that is easily absorbed by the body and incorporated into the body's iron stores. As a result, products using our core technology are well suited for use in intravenous iron replacement therapy.
374 articles about AMAG Pharmaceuticals
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AMAG Pharmaceuticals Announces FDA Approval of Supplemental New Drug Application (sNDA) for Feraheme (ferumoxytol injection)
2/5/2018
This sNDA approval immediately doubles the number of patients who could benefit from Feraheme to include both CKD and non-CKD patients.
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Here is a look at a few important regulatory events scheduled for the month of February.
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AMAG Pharmaceuticals Announces Preliminary 2017 Financial Results and Provides 2018 Guidance
1/8/2018
A live audio webcast of the presentation and following breakout session will be accessible through the Investors section of AMAG’s website.
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This is definitely a list few, if any, companies want to be on.
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New Patent Issued to AMAG Pharma Entitled "Methods of Reducing Risk of Preterm Birth"
12/20/2017
If approved, the auto-injector will join the Makena portfolio, which also includes the FDA-approved intramuscular injection.
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AMAG Announces Autologous Cord Blood Cells Improve Motor Function in Some Children With Cerebral Palsy
11/8/2017
More than one-third of study participants in Phase 2 Study were Cord Blood Registry (CBR) clients.
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Hypophosphatemia Data From AMAG Phase III Trial Presented at the American Society of Nephrology
11/6/2017
This study was comprised of approximately 2,000 adult patients with iron deficiency anemia regardless of the cause who had failed or could not tolerate oral iron therapy
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AMAG Pharmaceuticals Announces Third Quarter 2017 Financial Results and Business Highlights
11/2/2017
Total GAAP revenue for the third quarter of 2017 increased to $153.7 million, 7% higher than the same period last year.
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AMAG Pharmaceuticals to Host Third Quarter 2017 Financial Results Conference Call and Webcast on Thursday, November 2, 2017 at 8:00 a.m. ET
10/19/2017
Management will host a conference call and webcast at 8:00 a.m. ET to discuss the results and provide an update on recent corporate developments.
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AMAG Appoints Tracy Palmer Berns As Chief Compliance Officer
9/29/2017
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AMAG Appoints Laura Williams, M.D. As Senior Vice President Of Clinical Development
9/7/2017
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AMAG Announces FDA Filing Acceptance And Six-Month Review Of Feraheme (Ferumoxytol) For The Treatment Of All Adult Patients With Iron Deficiency Anemia
8/31/2017
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AMAG Appoints Oscar Sanchez As Vice President Of Quality
8/8/2017
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AMAG Completes Feraheme (Ferumoxytol) FDA Submission For The Treatment Of All Adult Patients With Iron Deficiency Anemia
8/3/2017
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AMAG Announces Second Quarter 2017 Financial Results And Provides Corporate Update
8/3/2017
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AMAG Launches Intrarosa (Prasterone) In The U.S. – A Novel Product To Treat Moderate To Severe Dyspareunia Due To Menopause
7/24/2017
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AMAG To Host Second Quarter 2017 Financial Results Conference Call And Webcast On Thursday, August 3, 2017 At 8:00 A.M. ET
7/20/2017
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AMAG Announces U.S. FDA Filing Acceptance Of Supplemental New Drug Application For Makena® (Hydroxyprogesterone Caproate Injection) Subcutaneous Auto-Injector
6/26/2017
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AMAG Announces First Patient Enrolled In Phase IIb/IIIa Digoxin Immune Fab Study Conducted By Velo Bio
6/1/2017
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AMAG Appoints Helen Milton, Ph.D. As Vice President Of Regulatory Affairs
5/16/2017