Pharmaceutical APIs
sodium amidotrizoate
sodium ascorbate
sodium bicarbonate
sodium chloride
sodium citrate
sodium citrate dihydrate
sodium cromoglicate
sodium dihydrogen phosphate
sodium dihydrogen phosphate dihydrate
sodium feredetate trihydrate
sodium fluoride
sodium fusidate
sodium gluconate
sodium glycerophosphate
sodium hydrogen carbonate
sodium hydroxide
sodium iodide I 123
sodium lactate
sodium lauryl ether sulfate
sodium lauryl ether sulfo-succinate
sodium lauryl sulfoacetate
sodium molybdate
sodium molybdate dihydrate
sodium nitrite
sodium nitroprusside dihydrate
sodium oxybate
sodium phenylbutyrate
sodium picosulfate
sodium picosulfate monohydrate
sodium polystyrene sulfonate
sodium selenite
sodium selenite pentahydrate
sodium sulfate, anhydrous
sodium tetradecyl sulfate
sodium thiosulfate
sodium valproate
sodium zirconium cyclosilicate
sofosbuvir
solifenacin succinate
solriamfetol hydrochloride
somapacitan
somatrogon
somatropin
sorafenib tosilate
sotalol hydrochloride
Sotatercept
sotorasib
sotrovimab
soya bean oil, refined
soya oil
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