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c/compounding·submitted 2 years ago by u/marit_mwangi

reading telehealth threads from 2024 and half of it aged badly

Pricingbranch of 7 comments

Long-ish post, sorry. tl;dr at the bottom. I have been tracking state board against eGFR for 35 weeks because I could not find anyone who had. The correlation is weaker than I expected, which is itself mildly interesting given how confidently people link the two in here. Caveats up front: one person, one lab, one…

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7 comments, started 2 years ago
u/bilal_osei41 points·2 years ago

API transparency is the question that separates good compounders from sketchy ones

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u/camila_sandvik27 points·2 years ago

Yeah, 503A and 503B are different regulatory animals.

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u/rania_diallo8 points·2 years ago

Did they tell you their API source or dodge the question?

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u/lipid_panel_larrybloodwork9 points·2 years ago

Not convinced. The evidence does not support that reading.

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u/julia_erdogan7 points·2 years ago

You have restated the marketing copy. What is the actual substance here.

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u/dario_stanescu5 points·2 years ago

This is correct. The shortage list does expire and the rules change.

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u/lift_heavy_thingsresistance training14 points·2 years ago

Yeah, 503A and 503B are different regulatory animals.

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About c/compounding

Compounded GLP-1s as a supply route: the 503A/503B distinction, the shortage-list mechanics that made compounding legal and then didn't, state board rules, telehealth prescriber models, and what a compounding pharmacy will and will not tell you about its API source.

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c/compounding rules
  1. Regulatory claims need a citation to the actual rule, notice or docket.
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