Pharmaceutical APIs
cyclopentolate hydrochloride
cyclophosphamide
cyclophosphamide monohydrate
cycloserine
cyproterone acetate
cysteine
cytarabine
cytisine
dabigatran etexilate
dabigatran etexilate mesilate
dabrafenib mesilate
dacarbazine citrate
dacomitinib monohydrate
dactinomycin
dalbavancin hydrochloride
dalteparin sodium
danaparoid sodium
Danicopan
dantrolene sodium
dantrolene sodium hemiheptahydrate
dantron
Dapagliflozin
dapagliflozin propanediol monohydrate
dapoxetine hydrochloride
dapsone
daptomycin
daratumumab
darbepoetin alfa
daridorexant hydrochloride
darifenacin
darifenacin hydrobromide
darolutamide
darunavir
darunavir ethanolate
darunavir propylene glycolate
dasatinib
dasatinib monohydrate
daunorubicin
daunorubicin hydrochloride
decitabine
deferasirox
deferiprone
defibrotide
deflazacort
degarelix acetate
delafloxacin meglumine
Delgocitinib
delta-9-tetrahydrocannabinol
demeclocycline hydrochloride
dengue tetravalent vaccine (live, attenuated)
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