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ForumsPublic SquareCompounded sema shortage — my results so far

Compounded sema shortage — my results so far

mark_tokyo Sat, Aug 16, 2025 at 4:25 PM 32 replies 1,406 viewsPage 1 of 7
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mark_tokyo
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Tokyo, JP
Aug 16, 2025 at 4:25 PM#1

My pharmacy stopped supplying with three weeks notice and a letter that explained nothing, so I went and read the statute.

What I am after is what actually distinguishes 503A from 503B, in terms of what each may make and from what starting material.

If the honest answer is that nobody knows, that is a useful answer and I would rather have it.

31 1pete_manc_UK, anna.melb_AU, mark_tokyo and 28 others
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MikeFit_NJ
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6,543
Apr 2024
New Jersey
Aug 16, 2025 at 4:38 PM#2

Taking the question as asked, rather than the general version of it. They are two different exemptions from the same federal requirements and they buy different things. A 503A pharmacy is regulated primarily by the state board, needs a patient-specific prescription, is exempt from CGMP, and may use a bulk substance that has a USP monograph, is a component of an approved drug, or appears on the 503A bulks list — three independent doorways. A 503B outsourcing facility registers with the FDA, is inspected on a risk basis, must comply with CGMP, may compound for office stock without a patient-specific prescription, and has one doorway to a permitted bulk substance: the 503B bulks list, or the drug shortage list.

30 0marcus_mpls, DeniseRN_TPA, SandraNC_45 and 27 others
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DebRD_ATL
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Feb 2024
Atlanta, GA
Aug 16, 2025 at 4:51 PM#3
MikeFit_NJ said:
They are two different exemptions from the same federal requirements and they buy different things.

That is correct as far as it goes, and here is where it stops going. Worth adding the genuine exception, because it is real and narrow: a change made for an identified patient where the prescriber determines it produces a significant clinical difference for that patient. A grid of fixed doses offered to everybody is not that, whatever the intake form says.

29 24SleepDoc_PDX, RegAffairsDC, BiostatsBrad and 26 others
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maria_elpaso
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Sep 2024
El Paso, TX
Aug 16, 2025 at 5:04 PM#4
mark_tokyo said:
My pharmacy stopped supplying with three weeks notice and a letter that explained nothing, so I went and read the statute.

This matches mine closely enough to be worth saying so. Resolution therefore closed the doors unevenly, and the asymmetry follows from the bulks lists. For 503B the shortage clause was the only route to these molecules, so that route shut completely. A 503A pharmacy can still argue a doorway via "component of an approved drug" — but only for the substance in the form present in the approved product, which is exactly where the base-versus-salt argument lives, and it does nothing about the copy restriction, which came back into force on resolution.

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Dr.RenalNash
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Mar 2024
Nashville, TN
Aug 16, 2025 at 6:15 PM#5

Adding the clinical framing, because it changes how the question reads.

Vendor communication red flags for compounded supply:

  • Won't provide COA before purchase — walk away
  • Claims "100% pure" without analytical data — unrealistic
  • No physical address or phone number — accountability matters
  • Pushes you to buy more than you need — pressure tactics
  • Won't answer questions about their compounding process — transparency is key
  • Payment only via crypto or wire transfer — legitimate pharmacies accept cards

A legitimate compounding pharmacy operates like a healthcare business, not a gray market dealer.

27 22maria_elpaso, anders_CPH, Dr.NutriCornell and 24 others
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