Methylphenidate API Manufacturer India

Name: Methylphenidate
Brand: Mediocon Inc
Availability: InStock

Methylphenidate — Pharmaceutical Grade API

Product Overview

CAS No: 113-45-1 | MF: C₁₄H₁₉NO₂ | MW: 233.31 g/mol

Methylphenidate is a pharmaceutical-grade active ingredient classified as CNS Stimulant / ADHD. Mediocon Inc supplies high-purity Methylphenidate API conforming to IP / BP / EP / USP specifications, manufactured in our GMP-certified facility in Aurangabad, Maharashtra, India.

Key Features

Dopamine & norepinephrine reuptake inhibitor
IP/BP/EP/USP compliant
Full CoA and MSDS documentation
GMP certified manufacturing

Applications

Attention deficit hyperactivity disorder (ADHD)
Narcolepsy
Cognitive fatigue

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 NameMethylphenidate

Also Known AsRitalin; Concerta

CAS Number113-45-1

Chemical Namemethyl 2-phenyl-2-(piperidin-2-yl)acetate

Molecular FormulaC₁₄H₁₉NO₂

Molecular Weight233.31 g/mol

CategoryCNS Stimulant / ADHD

AppearanceWhite crystalline powder

SolubilityFreely soluble in water

GradeIP / BP / EP / USP

Analytical Specifications

Parameter	Specification
Assay	NLT 98.0%
Loss on Drying	NMT 0.5%
Heavy Metals	NMT 20 ppm
Residue on Ignition	NMT 0.1%
Microbial Limits	Complies with pharmacopoeia
Identification	IR, HPLC Compliant
Packing	25 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 Methylphenidate (CAS 113-45-1) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Methylphenidate 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 — Methylphenidate API

What is the minimum order quantity for Methylphenidate API?

Mediocon Inc supplies Methylphenidate 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 Methylphenidate does Mediocon supply?

We supply Methylphenidate 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 Methylphenidate API?

Every shipment of Methylphenidate 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 Methylphenidate bulk orders?

Standard lead time for Methylphenidate 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.

Company

Product Catalog

Methylphenidate API Manufacturer & Supplier in India

Product Overview

Product Specifications

Analytical Specifications

Sourcing, Regulatory & Export Information

Frequently Asked Questions — Methylphenidate API

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