Import Albendazole — Buy in Bulk from Supplier in China

Albendazole from Aurora Industry Co., Ltd. is an synthetic anthelmintic API with CAS number 54965-21-8 and AUCO number 906, supplied in 25 kg drums for bulk pharmaceutical manufacturing. The material is a benzimidazole derivative that functions by inhibiting tubulin polymerisation in parasitic worms, leading to impaired glucose uptake and eventual death of the parasite. This API is intended for formulation into finished dosage forms for human and veterinary use.

The typical chemical composition is C12H15N3O2S with a molecular weight of 265.33 g per mol, though buyers should request a current Certificate of Analysis to confirm the specific batch purity and impurity profile. Standard pharmaceutical grades require assay values of 98.0 per cent to 102.0 per cent on an anhydrous basis, with related substances controlled per ICH Q3A guidelines. The material is usually a white or almost white crystalline powder, practically insoluble in water and freely soluble in formic acid, with storage typically under cool, dry conditions protected from light. Common pharmacopoeial references include USP, BP and EP monographs for Albendazole, which specify identification by infrared absorption, chromatographic purity, and residue on ignition limits.

Formulators use this API in tablet and suspension formulations, commonly at 200 mg and 400 mg strengths for human anthelmintic therapy, and in veterinary boluses and feed premixes for livestock. Key buyer segments include generic pharmaceutical manufacturers, veterinary pharmaceutical companies, and contract manufacturing organisations serving tropical and developing markets where soil-transmitted helminthiases remain prevalent. Trade terms mentioned include FOB and CIF options, with flexible MOQ to be confirmed directly with Aurora Industry Co., Ltd. given the zero per cent response rate currently shown.

Aurora Industry Co., Ltd. is a China-based supplier positioned within the imported supplier tier and classified at harbour trust level. The listing provides no specific address, year of establishment, or manufacturing facility details. The response rate stands at zero per cent with an average response time of zero hours, indicating no historical engagement data is available through this channel. Buyers should treat direct communication as essential before advancing any commercial discussion.

The supplier profile does not state GMP certification, FDA registration, DMF availability, or any other regulatory filing status. No headcount, revenue figure, or client references are provided. The product description emphasises international pharmaceutical standards compliance without specifying which certifications are held. Verification of ISO status, GMP certification, and whether the site is subject to any regulatory inspection history should be requested directly from Aurora Industry Co., Ltd. before qualification.