Active Pharmaceutical Ingredient

Sumatriptan Succinate

Also known as: Imitrex Succinate; Sumatriptan Hydrogen Succinate

CAS: 103628-48-4 Serotonin Agonist / Antimigraine Salt IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Sumatriptan Succinate API — Mediocon Inc, Aurangabad Maharashtra India
Sumatriptan Succinate — Pharmaceutical Grade API | Mediocon Inc, Aurangabad, Maharashtra, India

Product Overview

CAS No: 103628-48-4  |  MF: C₁₄H₂₁N₃O₂S·C₄H₆O₄  |  MW: 413.49 g/mol

Sumatriptan Succinate is the succinate salt form of Sumatriptan, a selective serotonin receptor agonist for acute migraine treatment. The succinate salt is widely used in commercial tablet and injectable formulations. Mediocon Inc supplies pharmaceutical-grade Sumatriptan Succinate conforming to IP / BP / EP / USP specifications.

As the commercially preferred salt form, Sumatriptan Succinate offers excellent aqueous solubility and stability, making it suitable for both oral tablets and parenteral injection formulations used in the acute management of migraine and cluster headache.

Key Features

  • High-purity pharmaceutical grade API
  • IP / BP / EP / USP compliant
  • Full CoA and MSDS documentation
  • GMP certified manufacturing facility

Applications

  • Antimigraine tablet formulations
  • Injectable/subcutaneous preparations
  • Nasal spray manufacturing
  • Commercial pharmaceutical production

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 NameSumatriptan Succinate
Also Known AsImitrex Succinate; Sumatriptan Hydrogen Succinate
CAS Number103628-48-4
Molecular FormulaC₁₄H₂₁N₃O₂S·C₄H₆O₄
Molecular Weight413.49 g/mol
CategorySerotonin Agonist / Antimigraine Salt
AppearanceWhite to off-white crystalline powder
SolubilityFreely soluble in water
GradeIP / BP / EP / USP

Analytical Specifications

ParameterSpecification
AssayNLT 98.0%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 20 ppm
Residue on IgnitionNMT 0.1%
Microbial LimitsComplies with pharmacopoeia
IdentificationIR, HPLC Compliant
Mfg DateMAR 2025
Exp DateFEB 2031
Packing25 kg HDPE drums / as per requirement
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