Pharmaceutical APIs
eucalyptus oil
everolimus
evinacumab
evolocumab
exagamglogene autotemcel
exametazime
exemestane
exenatide
ex vivo expanded autologous human corneal epithelial cells containing stem cells
ezetimibe
factor II
factor IX
factor VII
factor VIII
factor VIII inhibitor bypassing activity
factor X
factor XIII
famciclovir
famotidine
fampridine
faricimab
febuxostat
febuxostat hemihydrate
febuxostat magnesium
fedratinib dihydrochloride monohydrate
felodipine
fenfluramine hydrochloride
fenofibrate
fentanyl
fentanyl citrate
Ferric carboxymaltose
ferric derisomaltose
ferric maltol
ferrous chloride
ferrous fumarate
ferrous gluconate
ferrous sulfate
fesoterodine fumarate
feverfew herb
fexofenadine hydrochloride
fezolinetant
fidaxomicin
filgotinib maleate
filgrastim
finasteride
finerenone
fingolimod hydrochloride
flavoxate hydrochloride
flecainide acetate
flucloxacillin sodium
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