genuine question about API source that I am slightly embarrassed to ask
Question in the title, detail here: genuine question about API source that I am slightly embarrassed to ask. Nothing in this thread is medical advice, and the choice between arrangements is one for you and a prescriber who knows your history. Concentration on the compounded vial was different from what I had been…
Same view. If the intake asked you nothing, the intake was a formality and you should factor that in.
the API source is the question nobody asks and everybody should
I would not read the price difference as a quality signal. Most of it is the consultation model, not the vial.
Who is the prescriber, and are they the same organisation as the pharmacy?
salt forms are the recurring argument and the answer is boring
Disagree — a 503B being registered does not make its preparations equivalent to an approved product. Different regulatory category entirely.
503A is patient-specific, 503B is outsourcing facility, they are not the same thing
That is not what patient-specific means. It refers to the prescription, not to a customisation of the formula.