| Towncrest Internal Medicine, Llp | |
|
2460 Towncrest Dr Iowa City IA 52240-6622 | |
| (319) 338-7862 | |
| Not Available |
| Full Name | Towncrest Internal Medicine, Llp |
|---|---|
| Speciality | Internal Medicine |
| Location | 2460 Towncrest Dr, Iowa City, Iowa |
| Authorized Official Name and Position | Steven Michael Cooper (ADMINISTRATOR) |
| Authorized Official Contact | 3193387862 |
| Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
| Mailing Address | Practice Location Address |
|---|---|
| Towncrest Internal Medicine, Llp 2460 Towncrest Dr Iowa City IA 52240-6622 Ph: (319) 338-7862 | Towncrest Internal Medicine, Llp 2460 Towncrest Dr Iowa City IA 52240-6622 Ph: (319) 338-7862 |
| NPI Number | 1720005424 |
|---|---|
| Provider Enumeration Date | 07/17/2006 |
| Last Update Date | 10/17/2007 |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1720005424 | NPI | - | NPPES |
| BCBS | Other | IA | BCBS GROUP NO. |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 207R00000X | Internal Medicine | (* (Not Available)) | Primary |
News Archive
Daiichi Sankyo Company, Limited (hereafter, Daiichi Sankyo) today announced that the U.S. Food and Drug Administration has approved SAVAYSA (edoxaban) Tablets, an oral, once-daily selective factor Xa-inhibitor, to reduce the risk of stroke and systemic embolism (SE) in patients with non-valvular atrial fibrillation (NVAF).
Centers for Medicare & Medicaid Services (CMS) Administrator Mark McClellan, M.D., Ph.D. today announced CMS will soon undertake a pilot program in partnership with hospitals in 13 states and the District of Columbia to determine the effectiveness of the voluntary compliance programs used by many hospitals.
In trauma patients with diabetes, poorer long-term control of blood glucose levels is linked to a higher risk of death and trauma-related complications, reports a study in SHOCK: Injury, Inflammation, and Sepsis: Laboratory and Clinical Approaches, Official Journal of the Shock Society.
The Cystic Fibrosis Foundation has announced its support of the Food and Drug Administration's (FDA) requirement that manufacturers of pancreatic enzyme replacements obtain FDA approval for their products within the next four years.
› Verified 8 days ago
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