Active Pharmaceutical Ingredient

Budesonide API Manufacturer & Supplier in India

Also known as: Pulmicort, Rhinocort (brand)

CAS: 51333-22-3 Corticosteroid USP / BP / IP Bulk Supply Available
Budesonide API Manufacturer India | Mediocon Inc
Budesonide — Pharmaceutical Grade API

Product Overview

CAS No: 51333-22-3  |  MF: C₂₅H₃₄O₆  |  MW: 430.53 g/mol

Budesonide is a synthetic corticosteroid with potent anti-inflammatory activity used for asthma (oral inhalation), allergic rhinitis (nasal spray), and inflammatory bowel disease (oral). It acts locally with minimal systemic effects. Mediocon Inc supplies pharmaceutical-grade Budesonide meeting IP/BP/EP/USP standards.

Key Features

  • Potent synthetic corticosteroid
  • IP/BP/EP/USP compliant quality
  • Asthma, rhinitis, and IBD treatment
  • Available for inhalation, nasal, and oral use

Applications

  • Inhalation aerosols and nebulizers
  • Nasal sprays for rhinitis
  • Oral capsules for Crohn's disease
  • Rectal foam and enema formulations

Why Choose Mediocon

  • ISO 9001:2015 & GMP certified manufacturing
  • Consistent batch-to-batch quality with full CoA
  • Export-ready documentation: COO, MSDS, DMF
  • Flexible MOQ for both R&D and commercial scale
  • Dedicated QA support for regulatory filings

Product Specifications

Product NameBudesonide
Also Known AsPulmicort, Rhinocort (brand)
CAS Number51333-22-3
Molecular FormulaC₂₅H₃₄O₆
Molecular Weight430.53 g/mol
CategoryCorticosteroid / Anti-inflammatory
AppearanceWhite to Off-White Crystalline Powder
GradeIP / BP / EP / USP

Analytical Specifications

ParameterSpecification
Assay97.0% – 103.0%
Loss on DryingNMT 0.5%
CAS No51333-22-3
Heavy MetalsNMT 10 ppm
StorageStore below 30°C
Packing25 kg HDPE drums / as per requirement

Sourcing, Regulatory & Export Information

Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Budesonide (CAS 51333-22-3) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Budesonide 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 — identity (IR/HPLC), assay, related substances, residual solvents (ICH Q3C), heavy metals, and microbial limits — before release with a Certificate of Analysis.

Export Markets

  • USA — FDA-registered facility; DMF support available for ANDA/NDA filings
  • Europe — EMA-compliant documentation; CEP/EDMF support on request
  • Africa & Middle East — WHO-GMP certified; competitive pricing for emerging markets
  • Southeast Asia — established logistics network; temperature-controlled shipments
  • India domestic — schedule H/X compliance; all state licensing documentation provided

Quality & Compliance

  • ISO 9001:2015 certified quality management system
  • GMP-certified manufacturing facility, Aurangabad, Maharashtra
  • Full batch traceability from raw material to finished API
  • Stability data available (ICH Q1A guidelines) for regulatory submissions
  • Dedicated QA team for customer audits and regulatory queries

Frequently Asked Questions — Budesonide API

What is the minimum order quantity for Budesonide API?
Mediocon Inc supplies Budesonide with a minimum order quantity of 1 kg (sample packs available for R&D). We accommodate both small R&D quantities and large commercial-scale orders. Contact our sales team at akshay@mediocon.com or +91 9309999757 for a tailored quote.
What pharmacopoeial grades of Budesonide does Mediocon supply?
We supply Budesonide conforming to IP / BP / EP / USP pharmacopoeial standards. Each batch is tested against full pharmacopoeial specifications and released with a Certificate of Analysis. Custom specifications can be accommodated for regulated markets.
What documentation is provided with Budesonide API?
Every shipment of Budesonide comes with: Certificate of Analysis (CoA), MSDS/SDS, Certificate of Origin (COO), and Drug Master File (DMF) support on request. We also provide GMP certification, ISO 9001:2015 compliance documentation, and full regulatory support for filings in USA (FDA), Europe (EMA), and other markets.
What is the lead time and shipping for Budesonide bulk orders?
Standard lead time for Budesonide is 2–4 weeks for standard orders; expedited shipments possible for urgent requirements. We ship to 40+ countries worldwide using approved pharmaceutical-grade packaging (25 kg HDPE drums / aluminium foil bags). All shipments include temperature-controlled logistics options where required by the product's storage conditions.
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