Targeted Drug Delivery - Leading the Future of Compounding
Our Pain Management Pharmacy Division compounds patient specific, high risk pain medication for
Intrathecal Pain Pump refills, IV bags, and Cassettes.
As a healthcare professional, you want the highest quality preparations that will
improve your patient’s quality of life.
You need a pharmacy that has the ability and dedication to provide high quality preparations that will treat your patients. AnazaoHealth Pain Management is the partner you need.
Scroll down to see our commitment to quality
Baclofen – up to 4,000 mcg/mL
Bupivacaine – up to 40 mg/mL (4%)
Clonidine – up to 6,000 mcg/mL
Fentanyl – up to 25,000 mcg/mL
Glycerin – any concentration up to 100%
Hydromorphone – up to 200 mg/mL
Ketamine – Call for available concentrations
Meperidine – up to 200 mg/mL
Methadone – up to 80 mg/mL
Morphine – up to 70 mg/mL
Phenol – any concentration up to 89%
Phenol / Glycerin Combination – up to 20% Phenol and 50% Glycerin
Ropivacaine – up to 10 mg/mL
Sufentanil – Call for available concentrations
Tetracaine – up to 20 mg/mL (2%)
The medications listed above are available in the following forms:
Cassettes: 50 cc, 100 cc, 250 cc
Intravenous (IV) Bags: 100 cc, 150 cc, 250 cc etc.
Syringes: 10 mL, 20 mL, 30 mL, 50 mL
Vials: 2 mL, 5 mL, 10 mL, 30 mL etc.
Dedicated Quality Assurance Team
Onsite Microbiology Department
Aseptic-Trained and experienced
Continuous training, monitoring, and testing
At AnazaoHealth, compounding sterile preparations is our specialty. We are appropriately licensed to provide pharmacy services in all 50 states, the District of Columbia, and selected U.S. territories. We offer a wide variety of preparations utilized by pain management physicians and clinics, physiatrists, neurologists, anesthesiologists, and hospitals.
THE AUTOCLAVE PROCESS
Now Offering Terminal Sterilization in
Combination with Aseptic Processing
We verify every terminal sterilization cycle with biological indicator proving at least 10 sterility assurance level. We use glass instead of plastic in autoclaving, so there is no risk of leaching when exposed to high temperatures.
Our internal Quality Assurance Control standards, along with external 3rd party testing, ensure our preparations meet or exceed all pharmacy standards and other regulatory requirements prior to dispensing.
Quarterly summary reports outline our performance against USP Chapter <797> compounding standards. All APIs are received from FDA-registered manufacturers or suppliers.
Customized Autoclaving extends BUD to 30 days at room temperature, maximizing sterility while still ensuring product potency and stability.
To Create and Provide the Most Powerful
Innovations in Healing for Our Patients
One of the largest Class 10,000 Clean Rooms available(ISO 7) that meet or exceed USP Chapter <797>guidelines
Sterile cGMP-compliant full coverall
Sterile face mask
Sterile wipes in all ISO areas
Sterile cleaning products in all ISO areas
Sporicidal used daily in all ISO 5 areas and at least twice monthly in ISO 7 and ISO 8 areas
Air and surface sampling performed daily in all ISO 5 areas
Potency, sterility and endotoxin test on every batch
Onsite Microbiology Department
Dedicated Quality Department
Positive-pressure-controlled compounding room to reduce particles
Certified laminar-air hoods, Class 100 (ISO 5) to provide unidirectional airflow
Multiple High-Efficiency Particulate Air (HEPA) filters.
Clean room and buffer room per USP Chapter <797>
For more information, or to place an
order, place call our Customer Service
Department at 800.995.4363 or email firstname.lastname@example.org