Pharmaceutical APIs
indapamide
indapamide hemihydrate
indigo carmine
indometacin
indoramin hydrochloride
infliximab
influenza vaccine
influenza vaccine (split virion, inactivated)
influenza vaccine (surface antigen, inactivated)
Influenza virus haemagglutinin
Influenza virus inactivated split (H1N1, H3N2-like, b/brisbane/60/2008-like, strains)
ingenol mebutate
inosine acedoben dimepranol
Inotersen sodium
inotuzumab ozogamicin
insulin aspart
insulin degludec
insulin detemir
insulin glargine
insulin glulisine
insulin lispro
interferon beta-1a
interferon beta-1b
interferon gamma-1b
iobenguane
iodine
iodixanol
iodoform
ioflupane
iohexol
iomeprol
iopamidol
ipilimumab
ipratropium bromide
ipratropium bromide monohydrate
iptacopan hydrochloride monohydrate
irbesartan
irbesartan hydrochloride
irinotecan hydrochloride trihydrate
irinotecan sucrosofate
iron
iron dextran
iron sucrose
isatuximab
isavuconazonium sulfate
isocarboxazid
isoflurane
isoleucine
isoniazid
isoprenaline hydrochloride
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