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ForumsCompounding & FormulationHas anyone dealt with is it normal for the powder to not fully dissolve? Page 2

Has anyone dealt with is it normal for the powder to not fully dissolve?

KarenAZ_mom Tue, Nov 18, 2025 at 4:29 PM 39 replies 1,964 viewsPage 2 of 8
TrialTracker_MD
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Jan 2024
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Nov 18, 2025 at 9:46 PM#6
Dr.NutriCornell said:
Resolution therefore closed the doors unevenly, and the asymmetry follows from the bulks lists.

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.

25 20Dr.EM_Chicago, pete_RVA, CarlaRPh_TPA and 22 others
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PharmacoVig_BOS
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Nov 18, 2025 at 11:50 PM#7
KarenAZ_mom 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…

Compounding pharmacy licensing verification for compounded supply: before ordering, verify your pharmacy's credentials:

  1. State Board of Pharmacy license — check on your state BOP website
  2. FDA registration (for 503B) — check on fda.gov
  3. DEA registration if handling controlled substances
  4. PCAB accreditation — voluntary but demonstrates commitment to quality
  5. USP <797>/<800> compliance for sterile compounding

This takes 10 minutes of research and could save you from receiving substandard or unsafe medication.

Last edited: Nov 19, 2025 at 2:50 AM
24 19Dr.GutHealth, amsterdam_pete, LondonLisa and 21 others
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Dr.BariatricHTX
Senior Member
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Houston, TX
Nov 19, 2025 at 1:54 AM#8
TrialTracker_MD said:
A research-chemical supplier selling lyophilised powder labelled research use only is not compounding and is not claiming to.

GMP compliance checklist relevant to compounded supply compounding quality:

  • Clean room environment with HEPA filtration
  • Environmental monitoring (viable and non-viable)
  • Personnel training and competency assessment
  • Validated analytical methods for testing
  • Stability testing program
  • Complete batch records and traceability
  • Quality management system with deviation handling

A 503B pharmacy following cGMP should be able to answer questions about ALL of these if you ask. Don't be afraid to ask — it's your health.

23 18Dr.EM_Chicago, pete_RVA, CarlaRPh_TPA and 20 others
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Sigma-Aldrich — Research-Grade Standards

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cory_ATX
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Jul 2024
Austin, TX
Nov 19, 2025 at 3:58 AM#9

A narrower follow-up, since the general answer is now clear:

What actually distinguishes 503A from 503B, in terms of what each may make and from what starting material?

22 17Dr.PathRoch, mona_PHX, andrew_nyc and 19 others
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KarenAZ_mom
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Scottsdale, AZ
Nov 19, 2025 at 1:55 PM#10

OP back with an update, since a thread like this is useless without one.

The bulks-list asymmetry was the piece I had missed entirely. It explains why one of my two pharmacies is still arguing it can supply and the other simply stopped.

2 2HPLC_Greg, LibrarianMeg
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