Pharmaceutical APIs
denosumab
dequalinium chloride
desferrioxamine mesilate
desflurane
desloratadine
desmopressin acetate
desmopressin acetate trihydrate
desogestrel
deucravacitinib
Deutivacaftor
dexamethasone
dexamethasone sodium metasulfobenzoate
dexamethasone sodium phosphate
dexamfetamine sulfate
dexibuprofen
dexketoprofen
dexketoprofen trometamol
dexmedetomidine hydrochloride
dexpanthenol
dexrazoxane
dexrazoxane hydrochloride
dextran 70
dextromethorphan hydrobromide
dextrose monohydrate
diamorphine hydrochloride
diazepam
diazoxide
dibrompropamidine isetionate
diclofenac diethylamine
diclofenac diethylammonium
diclofenac potassium
diclofenac sodium
dicycloverine hydrochloride
dienogest
diethylamine salicylate
diethylstilbestrol
difelikefalin acetate
digoxin
dihydrocodeine tartrate
diltiazem hydrochloride
dimenhydrinate
dimethyl fumarate
dimeticone
Dimeticone 350
dinoprostone
dinutuximab beta
diphenhydramine hydrochloride
diphtheria, tetanus and pertussis vaccine
diphtheria, tetanus and poliomyelitis
diphtheria, tetanus, pertussis (acellular) and poliomyelitis (inactivated)
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