Levodropropizine API is a synthetic, non-opioid antitussive agent belonging to the class of peripheral cough suppressants. It is the (S)-enantiomer of dropropizine and is primarily associated with the symptomatic treatment of cough. Unlike centrally acting opioid antitussives, Levodropropizine has a predominantly peripheral mechanism of action and is used in pharmaceutical formulations intended to reduce cough frequency and intensity.
Chemically, Levodropropizine is identified as (S)-3-(4-phenylpiperazin-1-yl)propane-1,2-diol. It has the molecular formula C₁₃H₂₀N₂O₂, molecular weight approximately 236.31 g/mol, and CAS number 99291-24-4. The stereochemical configuration is an important characteristic because Levodropropizine represents the S-enantiomer of dropropizine.
Levodropropizine is associated with peripheral antitussive activity and has been used in pharmaceutical preparations for the symptomatic management of dry and non-productive cough. Its peripheral action distinguishes it from centrally acting cough suppressants and makes it an established ingredient in cough-relief formulations in several markets.
MEDIOCON INC supplies Levodropropizine for applicable pharmaceutical manufacturing, formulation development, analytical research, quality-control testing and bulk API requirements, subject to product availability, regulatory requirements and batch-specific documentation.
| Parameter | Specification |
|---|---|
| Appearance | White or almost white crystalline powder |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Levodropropizine API Manufacturer & Supplier in India | MEDIOCON INC (CAS 99291-24-4) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Levodropropizine API Manufacturer & Supplier in India | MEDIOCON INC is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing before release with a Certificate of Analysis.
Export Markets
Quality & Compliance