B&B Pharmaceuticals, Inc. strives to provide the highest quality standards in the industry. First, we only purchase from facilities that follow current Good Manufacturing Procedures (cGMP) guidelines to certify that the material is processed with the utmost quality. All manufacturing facilities that we purchase from are registered with and inspected by the United States Food and Drug Administration and have their own National Drug Codes (NDC numbers).  These suppliers must pass our "Vendor Validation” process that includes a questionnaire, a QC of the COA and Manufacturing process, and then an evaluation of all API’s produced by said supplier. We routinely send out representatives to physically inspect each Manufacturing site to ensure the accuracy of the company’s claims and processes. When any product is initially received it is taken into our Class1000 cleanroom for a visual inspection by our QA manager to verify that there has been no external or internal damage to the containers that could implicate potential exposure. If a product has been found not acceptable it will be physically relabeled "rejected material” and the QA manager will refuse delivery of the product.  Any chemical that is deemed outdated, misbranded, counterfeit, adulterated, contaminated, or un-sellable prescription drugs shall be segregated from other drugs and either returned to the manufacturer or destroyed.  Finally, all products are shipped with up-to-date Material Safety Data Sheets. Certificates of Analysis are always available upon request or on our website through the C of A’s tab.  B&B is also licensed and inspected by the DEA, FDA and the Colorado Board of Pharmacy in compliance with state and federal regulations. 

B&B Pharmaceuticals, Inc. is a VAWD accredited wholesale distribution facility.