Active Pharmaceutical Ingredient

Sulfadiazine Sodium

Also known as: Sodium Sulfadiazine; Sulphadiazine Sodium

CAS: 547-32-0 Sulfonamide Antibiotic Salt IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Sulfadiazine Sodium API — Mediocon Inc, Aurangabad Maharashtra India
Sulfadiazine Sodium — Pharmaceutical Grade API | Mediocon Inc, Aurangabad, Maharashtra, India

Product Overview

CAS No: 547-32-0  |  MF: C₁₀H₉N₄NaO₂S  |  MW: 272.26 g/mol

Sulfadiazine Sodium is the sodium salt form of Sulfadiazine, offering improved water solubility for parenteral formulations. It is used for treating severe bacterial infections where oral administration is not feasible. Mediocon Inc supplies pharmaceutical-grade Sulfadiazine Sodium conforming to IP / BP / EP / USP specifications.

As a sulfonamide antibiotic, Sulfadiazine Sodium inhibits bacterial folate synthesis. The sodium salt is particularly important for intravenous and intramuscular injection formulations requiring good aqueous solubility.

Key Features

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

Applications

  • Injectable antibiotic formulations
  • IV infusion preparations
  • Hospital-grade pharmaceutical manufacturing
  • Severe infection treatment

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 NameSulfadiazine Sodium
Also Known AsSodium Sulfadiazine; Sulphadiazine Sodium
CAS Number547-32-0
Molecular FormulaC₁₀H₉N₄NaO₂S
Molecular Weight272.26 g/mol
CategorySulfonamide Antibiotic Salt
AppearanceWhite to off-white crystalline powder or granules
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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