Active Pharmaceutical Ingredient

Calanolide A API Manufacturer & Supplier in India

Antiviral IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India Export Worldwide
Calanolide A API — Mediocon Inc, Aurangabad Maharashtra India
Calanolide A — Pharmaceutical Grade API | Mediocon Inc, Aurangabad, Maharashtra, India

Product Overview

Calanolide A is a pharmaceutical-grade Active Pharmaceutical Ingredient (API) classified as a Antiviral. Antiviral agent with activity against HIV. Mediocon Inc supplies high-purity Calanolide A API conforming to IP / BP / EP / USP specifications from our GMP-certified manufacturing facility in Aurangabad, Maharashtra, India.

Our Calanolide A API undergoes stringent quality control testing including assay, related substances, residual solvents, heavy metals, and microbial limits before release. Each batch is accompanied by a full Certificate of Analysis and regulatory documentation.

Key Features

  • High-purity pharmaceutical grade API
  • IP / BP / EP / USP pharmacopoeial compliance
  • Full CoA, MSDS/SDS, and COO documentation per batch
  • GMP-certified manufacturing facility in Aurangabad, Maharashtra
  • Consistent batch-to-batch quality with HPLC verification
  • Export-ready packaging: 25 kg HDPE drums / aluminium foil bags

Why Choose Mediocon

  • ISO 9001:2015 & WHO-GMP certified manufacturing
  • Export to 40+ countries worldwide
  • Flexible MOQ: 1 kg (R&D sample) to 500+ kg commercial lots
  • Dedicated QA team for regulatory filings (US FDA, EMA, TGA)
  • Competitive pricing with short lead times from Aurangabad facility
  • Full regulatory support: DMF, CEP/EDMF on request

Product Specifications

Product NameCalanolide A
CategoryAntiviral
GradeIP / BP / EP / USP
AppearanceWhite to off-white crystalline powder
StorageStore below 25 °C, in a dry place, protected from light
Packing25 kg HDPE drums / aluminium foil bags / as per requirement
HS Code29419090
OriginAurangabad, Maharashtra, India

Analytical Specifications

ParameterSpecification
AssayNLT 98.0% (dried basis)
Loss on DryingNMT 0.5%
Heavy MetalsNMT 20 ppm
Residue on IgnitionNMT 0.1%
Related SubstancesComplies with pharmacopoeia
Microbial LimitsComplies with pharmacopoeia
IdentificationIR, HPLC Compliant
Packing25 kg HDPE drums / aluminium foil bags

Sourcing, Regulatory & Export Information

Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We supply Calanolide A and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

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 compliance; all state licensing documentation provided

Quality & Compliance

  • ISO 9001:2015 certified quality management system
  • WHO-GMP certified manufacturing facility, Aurangabad, Maharashtra
  • Full batch traceability — raw material to finished API
  • Stability data available (ICH Q1A guidelines) for regulatory submissions
  • Microbiological testing per USP <61> / <62> / BP 2.6.12

Frequently Asked Questions — Calanolide A API

What is the minimum order quantity for Calanolide A API?
Mediocon Inc supplies Calanolide A 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 us at akshay@mediocon.com or +91 9309999757 for a tailored quote.
What pharmacopoeial grades of Calanolide A does Mediocon supply?
We supply Calanolide A conforming to IP / BP / EP / USP pharmacopoeial standards. Each batch is tested against full pharmacopoeial specifications and released with a Certificate of Analysis.
What documentation is provided with Calanolide A API?
Every shipment 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 Calanolide A bulk orders?
Standard lead time is 2–4 weeks for standard orders; expedited shipments possible for urgent requirements. We ship to 40+ countries worldwide using approved pharmaceutical-grade packaging. Temperature-controlled logistics available where required.