Pharmaceutical APIs
ruxolitinib phosphate
sacituzumab govitecan
sacubitril
safinamide methansulfonate
salbutamol sulfate
salicylic acid
salmeterol xinafoate
salmonella enterica serovar typhi, ty21a
Salmonella typhi strain ty 21a
sapropterin dihydrochloride
sarilumab
SARS-CoV-2 recombinant spike protein
satralizumab
saxagliptin hydrochloride
sebelipase alfa
secukinumab
Seladelpar lysine dihydrate
selegiline hydrochloride
selenium
selexipag
selinexor
selpercatinib
selumetinib hydrogen sulfate
semaglutide
senna fruit extract
senna pods tinnevelly
sennoside
Sennoside B
serine
sertraline hydrochloride
setmelanotide
sevelamer carbonate
sevelamer hydrochloride
sevoflurane
sildenafil citrate
siltuximab
simeticone
simoctocog alfa
simvastatin
siponimod fumaric acid
sirolimus
sitagliptin
sitagliptin hydrochloride
sitagliptin hydrochloride monohydrate
Sitagliptin phosphate
sitagliptin phosphate monohydrate
sodium acetate trihydrate
sodium acid phosphate
sodium alginate
sodium alkylsulfoacetate
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