| Good Faith Wellness Center Pllc | |
|
2506 Lakeland Dr Ste 310 Flowood MS 39232-7640 | |
| (769) 487-6036 | |
| Not Available |
| Full Name | Good Faith Wellness Center Pllc |
|---|---|
| Speciality | Clinic/center - Multi-specialty |
| Location | 2506 Lakeland Dr Ste 310, Flowood, Mississippi |
| Authorized Official Name and Position | Michael L Bookhardt (AUTHORIZED OFFICIAL) |
| Authorized Official Contact | 7984876036 |
| Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
| Mailing Address | Practice Location Address |
|---|---|
| Good Faith Wellness Center Pllc 2506 Lakeland Dr Ste 310 Flowood MS 39232-7640 Ph: (769) 487-6036 | Good Faith Wellness Center Pllc 2506 Lakeland Dr Ste 310 Flowood MS 39232-7640 Ph: (769) 487-6036 |
| NPI Number | 1174387963 |
|---|---|
| Provider Enumeration Date | 02/12/2024 |
| Last Update Date | 02/12/2024 |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1174387963 | NPI | - | NPPES |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 261QM1300X | Clinic/center - Multi-specialty | (* (Not Available)) | Primary |
News Archive
Federal drug agents and one of the nation's biggest drug distributors are heading for a legal showdown that will test the government's strategy of going after larger corporations to fight rampant prescription drug abuse.
Vitamin D deficiency is associated with arterial stiffness, a risk factor for heart disease and stroke, in black teens according to a new study accepted for publication in The Endocrine Society's www.endo-society.org. Black teens taking vitamin D supplementation of 2,000 international units per day had a decrease in central arterial stiffness.
"The potential cost of pesticide-related illnesses in sub-Saharan African between 2005 and 2020 could reach $90 billion, according to a U.N. report released on Wednesday highlighting the growing health and environmental hazards from chemicals," the Associated Press/Guardian reports.
Human Genome Sciences, Inc. today announced that it has submitted a Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) for ZALBIN™ (albinterferon alfa-2b) for the treatment of chronic hepatitis C. The BLA submission includes the results of two pivotal Phase 3 clinical trials showing that 900-mcg albinterferon alfa-2b dosed every two weeks met its primary endpoint of non-inferiority to peginterferon alfa-2a (Pegasys) dosed once each week.
For the first time, scientists have developed a new risk score that can predict the 10-year risk of developing heart disease or having a stroke in persons aged 40 years or older in any world country.
› Verified 6 days ago
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