Treatment Pricing Options

Treatment Pricing Options

Dynamic filtering and sorting for all available medications

Please read this important information regarding Compounded Medication.

  • Compounded medications are tailored to meet the specific medical needs of individual patients when commercially available, FDA-approved drugs are not suitable. A compounded medication can be prescribed if a physician determines that there is a change, made for an identified individual patient, which produces, for that patient, a significant difference from the commercially available drug product.
  • Compounded medication is prepared by a licensed 503(a) or 503(b) pharmacy in accordance with applicable federal and state laws. Compounded drugs are not approved by the U.S. Food and Drug Administration (FDA), which means the FDA has not evaluated their safety, effectiveness, or quality prior to marketing.
  • Please be aware that compounded drugs may pose higher risks compared to FDA-approved products, including potential variability in strength, quality, and purity. Patients should consult with a healthcare provider to understand the potential benefits and risks associated with compounded medications.

We have access to a number of other pharmacies not listed below. "Do you have a preferred pharmacy? We regularly onboard new, proven pharmacies. Contact Us."

Currently as of 7/26, all pharmacies are operating on a 3-5 day turnaround time.

Still have questions? Email us at krewe@joinbigeasy.com or call us at 504-313-6301!
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Pharmacies like BPI, Nova, and ProRx are FDA registered 503(b) and/or Drug Manufacturers. They are held to the highest possible standards - FDA's 21 CFR part 210 and 211 (cMGP). They are inspected by the FDA, and their primary regulator is the FDA. They use the designated drug master file for their medications, every part of their raw material supply chain has to be FDA registered and inspected, and their variance in the medicine has to be next to none. They are held to the same standards as "brand name" drug manufacturers for their processes. Their BUDs have to be supported by testing and procedures audited by the FDA. There are only about 90 503bs in the US.

When a drug is in shortage 503(b)s can produce "essentially a commercial copy" to help meet demand. 503(b)s cannot manufacture new medication when the medication is no longer in shortage.

OptioRx and Miller's are 503(a)s. The 12,000 503as in the US are overseen by individual state boards of pharmacy, with wide ranges of enforcement and monitoring. 503as have very different standards. For example, not all states have adopted USP 797, in particular, Florida. 797 limits the BUD that you can put on a vial to 3 months, really 45 days. What that means is a vial made in Florida can be labeled with a 12 month BUD, while if it was made the same exact way in a neighboring state that did follow USP 797, it would have a 45 day BUD. 503as can have about a 10% variance in their manufacturing. Your 10mg script could be 9mg or 11mg. Individual 503(a)s can hold themselves to higher standards, but it's not required.

503(a)s can continue to produce compounded medication under specific guidelines as outlined by the FDCA.

Now - at the end of the day, 5mg of Tirz should work the same way regardless of where it's from. However, knowing what you are getting - the standards it's made to, the sterility, the efficacy, the integrity of the process - 503bs run circles around a 503a.
Pharmacy Status Medication BUD State Availability 12-week?
Ship entire quarter at once, pay at once
12-week, pay monthly?
Ship quarter at once, pay monthly
4-week, single payment?
Prescriptions under 8 weeks are charged at this rate
Notes Potential Benefits