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ForumsBuyer Beware⚠ Compounding pharmacies with FDA 483 observations — updated list

⚠ Compounding pharmacies with FDA 483 observations — updated list

FDA_TrackerJim Thu, May 21, 2026 at 10:56 AM 9 replies 517 viewsPage 1 of 2
FDA_TrackerJim
Senior Member
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Feb 2024
Rockville, MD
May 21, 2026 at 10:56 AM#1

Putting this up now rather than when I am certain, because by then it will not help anybody.

Two pharmacies quoted me last year, one describing itself as 503A and one as 503B, and I assumed 503B just meant bigger until both stopped within weeks of each other.

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.

What to check: Two things anyone can check: a state licence number for a 503A, and an FDA outsourcing-facility registration for a 503B. Both are publicly searchable, and a pharmacy unwilling to give you either has answered the question.

If your experience contradicts this, say so in the thread — I would rather be corrected here than have people act on a warning that does not hold.

40 10Dr.Martinez, mike_mod, SarahChen_PharmD and 37 others
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Dr.NateNeph
VIP Member
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Dec 2023
Houston, TX
May 21, 2026 at 11:03 AM#2
FDA_TrackerJim said:
Two pharmacies quoted me last year, one describing itself as 503A and one as 503B, and I assumed 503B just meant bigger until both stopped within…

FDA_TrackerJim has the substance of this right. The condition it depends on is worth stating. 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.

39 9NauseaFreeNow, SteveThurs, B12Beth and 36 others
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Dr.BariatricHTX
Senior Member
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Feb 2024
Houston, TX
May 21, 2026 at 11:10 AM#3
FDA_TrackerJim said:
Two pharmacies quoted me last year, one describing itself as 503A and one as 503B, and I assumed 503B just meant bigger until both stopped within…

Filing a mild objection. Mild because I might be wrong; an objection because nobody has addressed the case that does not fit. A research-chemical supplier selling lyophilised powder labelled research use only is not compounding and is not claiming to. It is a different legal universe with no pharmacy oversight, no patient relationship and no content guarantee, and conflating the two in these threads helps nobody.

Ask again with the specifics and you will get a better answer than this one.

38 8Dr.EM_Chicago, pete_RVA, CarlaRPh_TPA and 35 others
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james_edin
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Sep 2024
Edinburgh, UK
May 21, 2026 at 11:17 AM#4

Short answer first, then the reasoning. 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.

37 7oliver_london, tane_welly, Dr.PathRoch and 34 others
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CryptoCarl
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May 2024
Arizona
May 21, 2026 at 11:54 AM#5
Dr.NateNeph said:
The shortage clause is the answer to the second question and it is a subtraction rather than an addition.

Second this.

Last edited: May 21, 2026 at 3:54 PM
36 6ChrisMacros, KetoKyle, CanadaChris and 33 others
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