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ForumsCompounding & FormulationEndotoxin testing in compounded injectables — anyone have experience?

Endotoxin testing in compounded injectables — anyone have experience?

lucas_SP_BR Tue, Nov 12, 2024 at 2:58 AM 8 replies 1,672 viewsPage 1 of 2
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lucas_SP_BR
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Nov 12, 2024 at 2:58 AM#1

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

So the question, as narrowly as I can put it: why a shortage listing created a legal pathway at all, since a shortage is a supply fact rather than a permission.

Tell me what I have not thought of.

41 19NurseKim_ATL, paul_denver, TinaHashiRN and 38 others
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Dr.SportsMedIN
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Nov 12, 2024 at 3:07 AM#2

Short answer first, then the reasoning. The shortage clause is the answer to the second question and it is a subtraction rather than an addition. Both exemptions forbid compounding something that is essentially a copy of a commercially available approved product. A product FDA has listed as in shortage is not treated as commercially available, so listing removed the objection that otherwise blocked compounding. It never created a permission; it withdrew a prohibition, which is why it evaporated the moment the supply fact changed.

42 20lisa_labSD, adam_van, Dr.SurgeonPGH and 39 others
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LondonLisa
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Nov 12, 2024 at 3:16 AM#3
Dr.SportsMedIN said:
The shortage clause is the answer to the second question and it is a subtraction rather than an addition.

Agreed, and the enforcement dates were staggered by category — 503A first, 503B a few weeks later — because outsourcing facilities have manufactured inventory and clinic contracts to unwind while a 503A makes to order.

43 21RetaRick_CA, JenPlateau, SallyK_inj and 40 others
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Dr.EndoIndy
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Nov 12, 2024 at 3:25 AM#4
lucas_SP_BR said:
My pharmacy stopped supplying with three weeks notice and a letter that explained nothing, so I went and read the statute.

Can confirm the pattern lucas_SP_BR describes. 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.

44 22DeniseRN_TPA, SandraNC_45, Dr.EndoIndy and 41 others
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PedsEndoPhilly
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Nov 12, 2024 at 4:14 AM#5

From the other side of the consultation, briefly.

Regarding compounded supply compounding legality: compounding pharmacies can legally produce semaglutide and tirzepatide while these drugs remain on the FDA shortage list. If/when the shortage resolves, the legal landscape may change.

Stay informed. The FDA shortage list is updated regularly. Current status as of my last check: semaglutide shortage ongoing, tirzepatide partially resolved. This directly impacts compounding availability.

Last edited: Nov 12, 2024 at 9:14 AM
45 23MikeNYC_runner and 42 others
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