Credentialed & Compliant
American Wellness Pharmacy holds active licenses across multiple states and operates in full compliance with federal FDA regulations, USP compounding standards, and state board requirements. Transparency is foundational to how we operate.
Verify Our License → Provider PortalWhat This Means for You
Under Section 503A of the Federal Food, Drug, and Cosmetic Act, American Wellness Pharmacy operates as a patient-specific compounding pharmacy. This means every medication we produce is compounded for an identified individual patient based on a valid prescription from a licensed healthcare provider.
503A pharmacies are subject to state pharmacy board oversight, unlike 503B outsourcing facilities which operate under direct FDA oversight for bulk production. Our 503A status means stricter patient protections and a true one-on-one compounding relationship.
503A vs 503B: 503B facilities manufacture medications in bulk without patient-specific prescriptions. 503A pharmacies like AWP only compound for a specific, identified patient upon receipt of a valid prescription — a higher standard of personalized care.
Nevada Pharmacy License
Nevada State Board of Pharmacy — Active
Active
DEA Registration
Drug Enforcement Administration — Registered
Active
503A Compounding Classification
Federal FDCA Section 503A — Compliant
Compliant
Multi-State Coverage
We hold active pharmacy licenses in the following states, allowing us to compound and ship medications directly to patients in those states. Our licensing footprint continues to grow.
Nevada
Home State — Primary
Active
California
Non-Resident License
Active
Texas
Non-Resident License
Active
Florida
Non-Resident License
Active
Arizona
Non-Resident License
Active
Colorado
Non-Resident License
Active
Washington
Non-Resident License
Active
Oregon
Non-Resident License
Active
Illinois
Non-Resident License
Active
New York
Non-Resident License
Active
Pennsylvania
Non-Resident License
Active
Ohio
Non-Resident License
Active
Don’t see your state? We’re actively expanding. Contact us to check current coverage or ask about upcoming additions.
Regulatory Framework
AWP operates under a multi-layered compliance framework spanning federal law, state pharmacy board regulations, and industry best practices.
FDA Regulations — Section 503A FDCA
All compounding activities comply with Section 503A of the Federal Food, Drug, and Cosmetic Act. This governs which drugs may be compounded, prescription requirements, and ingredient sourcing from FDA-registered suppliers.
NABP Compliance
American Wellness Pharmacy follows National Association of Boards of Pharmacy (NABP) standards for non-resident pharmacy practices, including patient safety protocols and interstate shipping compliance.
USP <795> Non-Sterile Compounding
Our non-sterile compounding (capsules, creams, troches, topicals) follows USP Chapter 795 guidelines — covering personnel training, facility standards, beyond-use dating, and quality control.
USP <797> Sterile Compounding
All injectable and sterile preparations are produced in an ISO-classified cleanroom environment following USP Chapter 797 — including environmental monitoring, sterility testing, and strict beyond-use dating protocols.
DEA Registration — Controlled Substances
AWP holds current DEA registration for handling and compounding controlled substances, including testosterone and other Schedule III medications. All controlled substance handling follows DEA 21 CFR requirements.
Nevada State Board of Pharmacy Oversight
As our home-state licensing authority, the Nevada State Board of Pharmacy has jurisdiction over AWP’s compounding practices, pharmacist licensure, and facility standards. We maintain full compliance with all Nevada pharmacy statutes and regulations.
Quality Standards
Licensing is the floor, not the ceiling. Here’s how AWP goes beyond minimum requirements.
Sterile compounding is performed in an ISO-classified cleanroom with continuous environmental monitoring and particle counts to ensure contamination-free preparation.
We partner with accredited independent testing laboratories to verify potency, sterility, and identity of selected compounded preparations — beyond what regulations require.
All active pharmaceutical ingredients are sourced exclusively from FDA-registered suppliers with certificates of analysis. We are a PCCA member for access to the highest-purity bulk ingredients available.
Need to verify our pharmacy license for your records or compliance documentation? Contact us directly and we’ll provide current copies of all relevant licenses and certifications.
Stay Compliant Together
AWP actively monitors FDA updates, state board changes, and compounding legislation. Partner with us and stay ahead.
