Pharmaceutical APIs
morphine hydrochloride
morphine hydrochloride trihydrate
morphine sulfate
morphine sulfate pentahydrate
mosunetuzumab
moxifloxacin hydrochloride
moxonidine
mRNA-1273.167
Mrna encoding lp.8.1
mucopolysaccharide polysulfate
multivitamins
mumps vaccine
mupirocin
mupirocin calcium
mycophenolate mofetil
mycophenolate mofetil hydrochloride
mycophenolic acid as mycophenolate sodium
nabilone
nabumetone
nadolol
nafarelin acetate
naftidrofuryl oxalate
naldemedine tosylate
nalmefene hydrochloride dihydrate
naloxegol oxalate
naloxone hydrochloride
naloxone hydrochloride dihydrate
naltrexone hydrochloride
naphazoline hydrochloride
naproxen
naratriptan hydrochloride
natalizumab
nateglinide
nebivolol hydrochloride
nefopam hydrochloride
nelarabine
Nemolizumab
neomycin sulfate
neostigmine bromide
neostigmine methylsulfate
neostigmine metilsulfate
nepafenac
neratinib maleate
netarsudil mesylate
netilmicin
netilmicin sulfate
netupitant
nevirapine
nevirapine anhydrate
nevirapine hemihydrate
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