Active Pharmaceutical Ingredient

Amphotericin B API Manufacturer & Supplier in India

Also known as: Fungizone

CAS: 1397-89-3 Polyene Antifungal USP / BP Bulk Supply Available
Amphotericin B API Manufacturer India | Mediocon Inc
Amphotericin B — Pharmaceutical Grade API

Product Overview

CAS No: 1397-89-3  |  MF: C₄₇H₇₃NO₁₇  |  MW: 924.08 g/mol

Amphotericin B is a polyene macrolide antifungal agent produced by Streptomyces nodosus. It acts by binding to ergosterol in the fungal cell membrane causing increased permeability. Mediocon Inc supplies pharmaceutical-grade Amphotericin B meeting USP and BP standards for injectable and liposomal formulations.

Key Features

  • Broad-spectrum polyene antifungal
  • USP/BP compliant quality
  • Active against Candida, Aspergillus & Cryptococcus
  • Suitable for IV and liposomal formulations

Applications

  • Systemic fungal infection IV infusion
  • Cryptococcal meningitis treatment
  • Invasive aspergillosis management
  • Liposomal amphotericin B 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 NameAmphotericin B
Also Known AsFungizone
CAS Number1397-89-3
Molecular FormulaC₄₇H₇₃NO₁₇
Molecular Weight924.08 g/mol
CategoryPolyene Antifungal
AppearanceYellow to Orange Powder
GradeUSP / BP

Analytical Specifications

ParameterSpecification
AssayNLT 750 mcg/mg
Loss on DryingNMT 5.0%
Melting PointN/A
Heavy MetalsNMT 30 ppm
pH6.0 – 8.0 (0.1% solution)
Microbial LimitsComplies with pharmacopoeia
IdentificationIR, HPLC Compliant
Packing1 kg amber glass bottles / 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 Amphotericin B (CAS 1397-89-3) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Amphotericin B 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 — Amphotericin B API

What is the minimum order quantity for Amphotericin B API?
Mediocon Inc supplies Amphotericin B 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 Amphotericin B does Mediocon supply?
We supply Amphotericin B conforming to USP / BP 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 Amphotericin B API?
Every shipment of Amphotericin B 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 Amphotericin B bulk orders?
Standard lead time for Amphotericin B 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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