Uhh the inactive ingredients are the most important bit of information a person can have when extracting from pills. Using water on most pills nowadays will cause them to swell up and slowly release the active ingredient. Also the pills today can't just simply be ground to a powder and extracted with ethanol because of the matrix formulation of them. Meaning the shit holding onto the pseudoephedrine will still be holding onto it after a simple extraction. Doing an AB doesn't do anything either because the binder isn't bothered by pH. I don't know if it would crystalize correctly because of the binder, I doubt it though.
That binder/ polymer holding onto the pseudoephedrine needs to be dealt with before the pseudoephedrine is accessible and able to be reduced.
MCC is the first thing that pops out to me as the binder which causes it to swell. Also any pills that have a coating that is acting as a shell, like this pill, needs to be removed first. Otherwise it is going to just hinder what you're attempting to do.
Tetrachloroethylene might help you out.
The 3 types of matrix pills ("hydrophilic matrix" are also known as "dry matrix")
- Hydrophilic Matrix Tablets: These contain water-soluble polymers that swell in the presence of water, creating a gel layer that controls the drug release rate.
- Lipophilic Matrix Tablets: Made with water-insoluble polymers, these tablets release their contents by slowly eroding in the digestive tract.
- Bi-layer Matrix Tablets: These are composed of two layers with different release profiles, typically one immediate and one extended-release layer, allowing for dual drug release kinetics or fixed-dose combinations (two drugs in one tablet).
But no matter what do your research, there is a lot of information out there about how to get around MCC and how to successfully extract the pseudo. A person doesn't need to become a chemist to do this, but they need to understand 'why' so they know 'what' they are doing.