Iverson Corner Drug | |
408 Minnesota Ave Nw, Bemidji, Minnesota 56601 | |
(218) 444-3000 |
Name | Iverson Corner Drug |
---|---|
Organization Name | Iverson Corner Drug, Inc. |
Location | 408 Minnesota Ave Nw, Bemidji, Minnesota 56601 |
Type | Durable Medical Equipment & Medical Supplies Supplier |
Phone | (218) 444-3000 |
Participate in Medicare | Medicare enrolled and may accept medicare assignment. Please check with the supplier if they accept medicare-approved amount before you get your prescription drugs, equipment or supplies from this supplier. |
News Archive
Viking Systems, Inc. reported today that it officially launched its Next Generation 3DHD Visualization System on October 4, 2010 at the American College of Surgeons Clinical Congress (ACS) held October 3-7 in Washington, DC. The Company also announced today its first distribution partners for the new system.
Mobile health technology has the potential to transform the way we prevent and manage heart disease, but there are unanswered questions about how to optimize this technology and maintain engagement with patients, according to a review of randomized clinical trials published in the Canadian Journal of Cardiology.
Pharma Major Lupin Limited announced today that its US subsidiary, Lupin Pharmaceuticals Inc. (collectively Lupin) has launched the all new InspiraChamber Anti-Static Valved Holding Chamber (VHC) under a strategic licensing agreement with the New Jersey based respiratory research and development company InspiRX Inc.
Desk-Trainer Ltd., specialists in the development of the successful five minute interactive exercise programs, announces the launch of a new Swedish sub-site with 10 first exercises translated into Swedish designed to protect against pain and injury resulting from Repetitive Stress Injuries (RSI) or other physical activities. During the first 4 weeks Desk-Trainer will offer 5 exercises in Swedish FREE.
Dendreon Corporation today announced that it has completed the submission of the post-approval supplement to the PROVENGE® (sipuleucel-T) Biologics License Application for the Morris Plains, New Jersey manufacturing facility. Dendreon is requesting licensure for an additional 36 workstations to manufacture PROVENGE. The standard U.S. Food and Drug Administration (FDA) review for a post-approval supplement to a Biologics License Application is typically four months.
› Verified 1 days ago
NPI Number | 1184723611 |
Organization Name | IVERSON CORNER DRUG INC |
Doing Business As | IVERSON CORNER DRUG |
Type | Durable Medical Equipment & Medical Supplies Supplier |
Address | 408 Minnesota Ave Nw, Bemidji, MN 56601 |
Phone Number | 218-444-3000 |
News Archive
Viking Systems, Inc. reported today that it officially launched its Next Generation 3DHD Visualization System on October 4, 2010 at the American College of Surgeons Clinical Congress (ACS) held October 3-7 in Washington, DC. The Company also announced today its first distribution partners for the new system.
Mobile health technology has the potential to transform the way we prevent and manage heart disease, but there are unanswered questions about how to optimize this technology and maintain engagement with patients, according to a review of randomized clinical trials published in the Canadian Journal of Cardiology.
Pharma Major Lupin Limited announced today that its US subsidiary, Lupin Pharmaceuticals Inc. (collectively Lupin) has launched the all new InspiraChamber Anti-Static Valved Holding Chamber (VHC) under a strategic licensing agreement with the New Jersey based respiratory research and development company InspiRX Inc.
Desk-Trainer Ltd., specialists in the development of the successful five minute interactive exercise programs, announces the launch of a new Swedish sub-site with 10 first exercises translated into Swedish designed to protect against pain and injury resulting from Repetitive Stress Injuries (RSI) or other physical activities. During the first 4 weeks Desk-Trainer will offer 5 exercises in Swedish FREE.
Dendreon Corporation today announced that it has completed the submission of the post-approval supplement to the PROVENGE® (sipuleucel-T) Biologics License Application for the Morris Plains, New Jersey manufacturing facility. Dendreon is requesting licensure for an additional 36 workstations to manufacture PROVENGE. The standard U.S. Food and Drug Administration (FDA) review for a post-approval supplement to a Biologics License Application is typically four months.
› Verified 1 days ago
NPI Number | 1245964048 |
Organization Name | IVERSON CORNER DRUG INC |
Type | Long Term Care Pharmacy |
Address | 408 Minnesota Ave Nw, Bemidji, MN 56601 |
Phone Number | 218-444-3000 |
News Archive
Viking Systems, Inc. reported today that it officially launched its Next Generation 3DHD Visualization System on October 4, 2010 at the American College of Surgeons Clinical Congress (ACS) held October 3-7 in Washington, DC. The Company also announced today its first distribution partners for the new system.
Mobile health technology has the potential to transform the way we prevent and manage heart disease, but there are unanswered questions about how to optimize this technology and maintain engagement with patients, according to a review of randomized clinical trials published in the Canadian Journal of Cardiology.
Pharma Major Lupin Limited announced today that its US subsidiary, Lupin Pharmaceuticals Inc. (collectively Lupin) has launched the all new InspiraChamber Anti-Static Valved Holding Chamber (VHC) under a strategic licensing agreement with the New Jersey based respiratory research and development company InspiRX Inc.
Desk-Trainer Ltd., specialists in the development of the successful five minute interactive exercise programs, announces the launch of a new Swedish sub-site with 10 first exercises translated into Swedish designed to protect against pain and injury resulting from Repetitive Stress Injuries (RSI) or other physical activities. During the first 4 weeks Desk-Trainer will offer 5 exercises in Swedish FREE.
Dendreon Corporation today announced that it has completed the submission of the post-approval supplement to the PROVENGE® (sipuleucel-T) Biologics License Application for the Morris Plains, New Jersey manufacturing facility. Dendreon is requesting licensure for an additional 36 workstations to manufacture PROVENGE. The standard U.S. Food and Drug Administration (FDA) review for a post-approval supplement to a Biologics License Application is typically four months.
› Verified 1 days ago
News Archive
Viking Systems, Inc. reported today that it officially launched its Next Generation 3DHD Visualization System on October 4, 2010 at the American College of Surgeons Clinical Congress (ACS) held October 3-7 in Washington, DC. The Company also announced today its first distribution partners for the new system.
Mobile health technology has the potential to transform the way we prevent and manage heart disease, but there are unanswered questions about how to optimize this technology and maintain engagement with patients, according to a review of randomized clinical trials published in the Canadian Journal of Cardiology.
Pharma Major Lupin Limited announced today that its US subsidiary, Lupin Pharmaceuticals Inc. (collectively Lupin) has launched the all new InspiraChamber Anti-Static Valved Holding Chamber (VHC) under a strategic licensing agreement with the New Jersey based respiratory research and development company InspiRX Inc.
Desk-Trainer Ltd., specialists in the development of the successful five minute interactive exercise programs, announces the launch of a new Swedish sub-site with 10 first exercises translated into Swedish designed to protect against pain and injury resulting from Repetitive Stress Injuries (RSI) or other physical activities. During the first 4 weeks Desk-Trainer will offer 5 exercises in Swedish FREE.
Dendreon Corporation today announced that it has completed the submission of the post-approval supplement to the PROVENGE® (sipuleucel-T) Biologics License Application for the Morris Plains, New Jersey manufacturing facility. Dendreon is requesting licensure for an additional 36 workstations to manufacture PROVENGE. The standard U.S. Food and Drug Administration (FDA) review for a post-approval supplement to a Biologics License Application is typically four months.
› Verified 1 days ago
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