ZGNX Share Price

Open 10.30 Change Price %
High 10.45 1 Day 0.00 0.00
Low 10.00 1 Week -0.65 -5.91
Close 10.35 1 Month -0.25 -2.36
Volume 134256 1 Year 1.34 14.87
52 Week High 13.70
52 Week Low 7.33
ZGNX Important Levels
Resistance 2 10.77
Resistance 1 10.60
Pivot 10.27
Support 1 10.10
Support 2 9.93
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Zogenix, Inc. (NASDAQ: ZGNX)

ZGNX Technical Analysis 3
As on 22nd Mar 2017 ZGNX Share Price closed @ 10.35 and we RECOMMEND Buy for LONG-TERM with Stoploss of 9.98 & Buy for SHORT-TERM with Stoploss of 10.05 we also expect STOCK to react on Following IMPORTANT LEVELS.
ZGNX Target for March
1st Target up-side 12.21
2nd Target up-side 13.52
3rd Target up-side 14.83
1st Target down-side 8.49
2nd Target down-side 7.18
3rd Target down-side 5.87
ZGNX Other Details
Segment EQ
Market Capital 232515696.00
Sector Healthcare
Industry Drug Manufacturers - Major
Offical website http://www.zogenix.com
ZGNX Address
ZGNX
12400 High Bluff Drive
Suite 650
San Diego, CA 92130
United States
Phone: 858-259-1165
Fax: 858-259-1166
Interactive Technical Analysis Chart Zogenix, Inc. ( ZGNX NASDAQ USA )
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ZGNX Business Profile
Zogenix, Inc. (Zogenix) is a pharmaceutical company commercializing and developing products for the treatment of central nervous system disorders and pain. The Company�s product Sumavel DosePro offers needle-free subcutaneous administration of sumatriptan for the treatment of migraine and cluster headache in a pre-filled, single-use delivery system. Its lead product candidate, Zohydro (hydrocodone bitartrate, formerly ZX002) is a 12-hour extended-release formulation of hydrocodone without acetaminophen for the treatment of chronic pain requiring opioid therapy. It completed Phase 3 development of Zohydro in 2011. Sumavel DosePro and Zohydro are used for the treatment options available to patients and physicians in the United States. Its second DosePro investigational product candidate, Relday, is a injectable formulation of risperidone for the treatment of schizophrenia. In May, 2012, it submitted a New Drug Application to the Food and Drug Administration (FDA).