Physician Clinic

Cantrell Drug Company, a recognized leader in interventional pain management and high-risk sterile products, provides clinics, hospitals, and surgery centers with custom pain management pharmaceuticals, admixture services, research preparations, and other custom compounding services in both sterile and non-sterile dosage forms. All products are compliant with new U.S.P. Standards <797> and <795>.

Accredited by Pharmacy Compounding Accreditation Board
Pharm D. Clinical assistance available
On-site representative
Multi-state licensed
Registered DEA Manufacturer
Sterility test on EVERY intrathecal; both aerobic and anaerobic testing
Barcode verification of ingredients
Analytical balance integration with software to verify weights
Pharm D. Quality Control Director
Major hospital affiliations for sterile product compounding
University of Arkansas Medical Sciences College of Pharmacy teaching site
University of Arkansas Pharm. D. “industrial pharmacy track” cooperative educational partnership under development
9 check points at order entry for intrathecals
12 check points of compounding steps for intrathecals (including pH and osmotic/tonicity calculations)
3 check points of sterilization for intrathecals (including dual filtrations)
Tamper Resistant packaging
Ultraviolet protective packaging
Absolute compliance with DEA Regulations
6 check points of final product
5 check points for proper distribution (including temperature protective packaging)
Documented Quality Control Program

INTRATHECAL PAIN MANAGEMENT

U.S.P. <797> Compliant

Pain Management Product Listing

PCAs | Epidurals | Intrathecals

Available in: Deltec Cassettes, Hospira Vials, Flexible Bags, Syringes Products sealed tamper resistant and UV protected
Baclofen
Bupivacaine
Clonidine
Droperidol
Hydromorphone
Fentanyl
Meperidine
Methadone
Morphine
Prialt
Ropivacaine
Sufentanil
Tetracaine
Other products available upon request

DEA Registered Manufacturer

A common misunderstanding in the healthcare community is that a prescription may be utilized to acquire or distribute compounded controlled drugs from one DEA registrant to another (i.e. pharmacy to physician). This practice is prohibited by Federal Law. In addition, pharmacies, both retail and home health, are prohibited from utilizing not only a prescription, but also the DEA 22 form to compound narcotics for another DEA registrant. This transaction requires the services of a registered DEA manufacturer.

As a licensed DEA Manufacturer, Cantrell Drug can compound and distribute controlled substances to physicians and healthcare institutions for their office use and administration. All compounding and distribution is performed in strict compliance with DEA regulations.

Cantrell Drug Quality Assurance

U.S.P. <797> Compliant
Our Quality Assurance Program focuses on compliance with USP Guidelines on Pharmaceutical Compounding - Sterile Preparations, as well as recommendations from ASHP (American Society of Hospital Pharmacists) and NABP (National Association of Boards of Pharmacy). Accredited by PCAB - www.pcab.org

Compounding Personnel

Licensed Doctors of Pharmacy
Certified Pharmacy Technicians
American Society of Health System Pharmacists Aseptic Training
Validation of Technique
Routine Microbial Monitoring of Garb and Gloves
Ongoing Documentation
- Certified Class 100 Rooms
- Routine Air Sample Microbial Monitoring
- Routine Surface Microbial Monitoring

Compounding Environment

Independent Certification Class 100 (ISO 5)
Clean Rooms 164 Square Feet of Laminar Flow
0.2 Micron HEPA Filtered Air; Positive Pressure ISO 5 Rooms
Designated Sterile Product Laboratories
Acrylic Coated Aluminum Walls & Ceiling Grids
Fully Gowned Personnel

Product Testing

Independent FDA Registered Lab and In-House Testing per USP Guidelinesv
Sterility Testing Performed on 100% of Batch Lots
Endotoxin Texting – 100% of high-risk parenterals
Quantitative Analysis - 100% of high-risk parenterals

Quality is the objective of all processes involved in the compounding of sterile drug products. Cantrell Drug Company is constantly evaluating current compounding and testing procedures in order to continuously improve the quality of compounded sterile products to meet the needs of healthcare facilities, physicians, and patients.

Intrathecals

Click here for more information of Intrathecals.

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Rapid Microbiology

Appropriate end-product testing, including sterility testing, is performed according to USP ‹797› guidelines. Rapid Microbiology via Laser Scanning Cytometry is offered for most aqueous solutions, providing immediate, same-day sterility results-accurate down to one single microbe. Quantitative analysis is performed per USP requirements on each batch to determine concentration of the active ingredient(s). Potency testing is performed by an independent, FDA registered laboratory.

Office Use Meds

Intrathecal Custom Mixtures
PC Admixtures
Epidural Admixtures
Labor and Delivery Admixtures
Cardioplegias
Small Volume Vials
Small Volume Admixtures
Large Volume Admixtures
Steroid Injections
Special Request Sterile Products

Featured Products

Featured Product - Compounded Sulphan Blue

Non-Sterile Products

Custom medications for most any dosage form

CSOS

Controlled Substance Ordering System (CSOS)

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