Pharmaceutical APIs
protease
protein c
protein s
proxymetacaine hydrochloride
prucalopride succinate
pseudoephedrine hydrochloride
pumilio pine oil
pyrazinamide
pyridostigmine bromide
pyridoxine
pyridoxine hydrochloride
pyrimethamine
quetiapine fumarate
quetiapine hemifumarate
quinagolide hydrochloride
quinine bisulfate
quinine sulfate
quizartinib dihydrochloride
rabbit anti-human thymocyte immunoglobulin
rabeprazole sodium
rabies vaccine
Rabies virus (inactivated, strain flury lep)
racemic camphor
radium-223 dichloride
raloxifene hydrochloride
raltegravir
raltegravir potassium
raltitrexed
ramipril
ramucirumab
ranibizumab
ranitidine hydrochloride
ranolazine
rasagiline hemitartrate
rasagiline mesilate
rasagiline tartrate
rasburicase
ravulizumab
raxtozinameran
reboxetine
recombinant cholera toxin b subunit
regadenoson
regorafenib
relatlimab
relebactam monohydrate
relugolix
remdesivir
remifentanil hydrochloride
remimazolam besylate
repaglinide
About Pharmaceutical APIs
Active Pharmaceutical Ingredients (APIs) are the active substances in pharmaceutical drugs that produce the intended therapeutic effects. These chemical compounds undergo rigorous testing and quality control to ensure safety, efficacy, and consistency in drug formulations.
API Resources
Related Information
Did You Know?
API Quality Matters: The purity and quality of Active Pharmaceutical Ingredients directly impact drug safety and efficacy. All APIs must meet strict regulatory standards set by organizations like PPB Kenya and international pharmacopoeias.
Quick Facts
- APIs can be synthetic, semi-synthetic, or natural compounds
- Quality control includes identity, strength, and purity testing
- Must comply with Good Manufacturing Practices (GMP)
- Proper storage conditions are critical for API stability