Pharmaceutical APIs
hyaluronidase
hydralazine hydrochloride
Hydrated disodium ceftriaxone
hydrochlorothiazide
hydrocortisone
hydrocortisone acetate
hydrocortisone butyrate
hydrocortisone sodium phosphate
hydrocortisone sodium succinate
hydrogen peroxide
hydromorphone hydrochloride
hydroxocobalamin
hydroxocobalamin acetate
hydroxycarbamide
hydroxychloroquine sulfate
hydroxyzine hydrochloride
hyetellose
hyoscine
hyoscine butylbromide
hyoscine hydrobromide
hypromellose
hyssop liquid extract
ibandronic acid, monosodium salt, monohydrate
ibandronic sodium monohydrate
ibrutinib
ibuprofen
ibuprofen lysine
ibuprofen sodium
ibuprofen sodium dihydrate
icatibant acetate
icodextrin
icosapent ethyl
idarubicin hydrochloride
idarucizumab
idebenone
Idecabtagene vicleucel
idelalisib
idursulfase
ifosfamide
iloprost trometamol
imatinib mesilate
imiglucerase
imipenem monohydrate
imipramine hydrochloride
imiquimod
imlifidase
immunoglobulin
inclisiran sodium
indacaterol acetate
indacaterol maleate
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