Pharmaceutical APIs
diphtheria, tetanus, pertussis (acellular), hib vaccine and poliomyelitis
diphtheria, tetanus, pertussis (acellular), poliomyelitis (inactivated), hepatitis b (rDNA) and haemophilus influenzae type b (Hib) vaccine
dipipanone hydrochloride
dipyridamole
diroximel fumarate
disodium clodronate
disodium hydrogen citrate
disodium levofolinate
disodium phosphate
disodium phosphate dodecahydrate
disopyramide
disopyramide phosphate
disulfiram
dl-alpha-tocopherol
dl-alpha-tocopheryl acetate
dobutamine hydrochloride
docetaxel
docetaxel anhydrous
docusate sodium
dolutegravir sodium
domperidone
domperidone maleate
donanemab
donepezil hydrochloride
donepezil hydrochloride monohydrate
dopamine hydrochloride
doravirine
dornase alfa
dorzolamide hydrochloride
dostarlimab
dosulepin hydrochloride
doxapram hydrochloride
doxazosin mesilate
doxepin hydrochloride
doxorubicin hydrochloride
doxycycline hyclate
doxycycline monohydrate
doxylamine succinate
dried ferrous sulfate bp
dronedarone hydrochloride
droperidol
drospirenone
dulaglutide
duloxetine hydrochloride
dupilumab
durvalumab
dutasteride
dydrogesterone
echinacea purpurea
econazole nitrate
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