Pharmaceutical APIs



betamethasone

betamethasone dipropionate

betamethasone sodium phosphate

betamethasone valerate

betaxolol hydrochloride

Betula pendula Roth, Betula pubescens Ehrh. (as dry extract, refined)

bevacizumab

Bevacizumab gamma

bexarotene

bicalutamide

bictegravir sodium

bifonazole

bilastine

bimatoprost

bimekizumab

binimetinib

bisacodyl

bismuth oxide

bismuth subcitrate potassium

bismuth subgallate

bismuth subnitrate

bisoprolol fumarate

bivalirudin

black cohosh

bleomycin sulfate

blinatumomab

bortezomib mannitol boronic ester

bosentan monohydrate

Bosutinib

bosutinib monohydrate

botulinum toxin type a

brentuximab vedotin

bretovameran

brexucabtagene autoleucel

brigatinib

brimonidine tartrate

brinzolamide

brivaracetam

brodalumab

brolucizumab

bromfenac sodium sesquihydrate

bromocriptine mesilate

buclizine hydrochloride

budesonide

bulevirtide acetate

bumetanide

bupivacaine

bupivacaine hydrochloride

bupivacaine hydrochloride anhydrous

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.

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