Pharmaceutical APIs
potassium bicarbonate
potassium chloride
potassium citrate
potassium clavulanate
potassium dihydrogen phosphate
potassium hydrogen carbonate
potassium hydroxide
potassium hydroxyquinoline sulfate
potassium iodate
potassium iodide
potassium para-aminobenzoate
potassium phosphate dibasic
povidone iodine
pralsetinib
pramipexole dihydrochloride monohydrate
prasterone
prasugrel
prasugrel besilate
prasugrel hydrobromide
prasugrel hydrochloride
pravastatin sodium
prazosin hydrochloride
precipitated sulfur
prednisolone
prednisolone acetate
prednisolone hexanoate
Prednisolone metasulphobenzoate sodium
prednisolone sodium metasulfobenzoate
prednisolone sodium phosphate
pregabalin
prilocaine
prilocaine hydrochloride
primidone
procaine hydrochloride
procarbazine hydrochloride
prochlorperazine maleate
prochlorperazine mesilate
procyclidine hydrochloride
progesterone
proguanil hydrochloride
proline
promazine hydrochloride
promethazine hydrochloride
propafenone hydrochloride
propamidine isetionate
propantheline bromide
propofol
propranolol hydrochloride
propylthiouracil
protamine sulfate
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