Cefuroxime Sodium API Manufacturer in Maharashtra, India

Cephalosporin Antibiotic – Manufacturer and Bulk Supplier in Maharashtra for Antibacterial Oral And Parenteral Formulations

Cefuroxime Sodium API Manufacturer and Bulk Supplier in Maharashtra, India – Swapnroop Pharma

Product Specifications

Product Name: Cefuroxime Sodium API
CAS Number: 56238-63-2
Category: Active Pharmaceutical Ingredient
Grade: Cefuroxime Sodium IP / BP / EP / USP
Appearance: White to off-white crystalline powder
Standards: IP / BP / EP / USP compliant

Detailed Specifications

ParameterSpecification
AppearanceWhite to off-white crystalline powder
IdentificationIR & HPLC compliant
Assay (HPLC)98.0% – 102.0%
Loss on DryingNMT 1.0%
Residue on IgnitionNMT 0.2%
Heavy MetalsNMT 10 ppm
pH (1% Solution)2.0 – 4.0
Individual Impurity≤ 0.5%
Total Impurities≤ 1.5%

Cefuroxime Sodium API (CAS No: 56238-63-2)

WHO-GMP Certified Cefuroxime Sodium API Manufacturer in Maharashtra, India

Cefuroxime Sodium API (CAS 56238-63-2) is an Active Pharmaceutical Ingredient used in the formulation of prescription and/or over-the-counter pharmaceutical products. Swapnroop Drugs and Pharmaceuticals manufactures and supplies Cefuroxime Sodium API with pharmacopeial compliance (IP/BP/EP/USP as applicable) from our WHO-GMP certified facility in Aurangabad (MIDC Shendra), Maharashtra — one of India's premier pharmaceutical manufacturing zones with robust regulatory infrastructure.

Pharmaceutical formulation companies sourcing Cefuroxime Sodium API require consistent polymorphic or salt form characterisation, batch-to-batch HPLC purity ≥98% (or per specific pharmacopeial monograph), validated residual solvent control per ICH Q3C, and full impurity profiling against pharmacopeial limits. Our quality control laboratory performs complete pharmacopeial testing with USP/EP/IP validated analytical methods before every batch release.

Swapnroop's Cefuroxime Sodium API supply is backed by WHO-GMP certified manufacturing, a qualified vendor documentation package (CoA, MSDS, Certificate of Origin, stability data), and dedicated technical support for domestic formulation companies and international export customers. We maintain inventory for rapid order fulfilment across 25+ countries served from our Aurangabad facility.

Key Features

  • HPLC purity ≥98.0% (or per specific IP/BP/USP monograph for Cefuroxime Sodium)
  • Complete pharmacopeial testing: identification, assay, impurities, LOD, residue on ignition
  • Residual solvent control per ICH Q3C with validated GC/headspace methodology
  • WHO-GMP certified batch with full documentation package for regulatory submissions

Applications

  • Pharmaceutical tablet and capsule formulation development using Cefuroxime Sodium API
  • Injectable or parenteral formulation programs where Cefuroxime Sodium is indicated
  • R&D, pilot batch, and commercial manufacturing for domestic and regulated markets
  • Fixed-dose combination (FDC) drug product development programs

Why Choose Swapnroop for Cefuroxime Sodium?

  • WHO-GMP certified Aurangabad facility with CDSCO-approved manufacturing unit
  • Complete qualified vendor documentation: CoA, MSDS, CoO, stability reports
  • Export capability to 25+ countries with pharmacopeial-grade API
  • Responsive technical support and dedicated account management for long-term buyers

Packaging & Supply

Cefuroxime Sodium API is supplied in double-polyethylene-lined HDPE drums or fiber drums (25 kg net) with desiccant and nitrogen head-space. Smaller quantities (1 kg, 5 kg) in sealed HDPE jars for R&D programs. All packaging labelled with batch, grade, and pharmacopeial standard.

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Frequently Asked Questions about Cefuroxime Sodium API

What is the CAS number for Cefuroxime Sodium API?

The CAS number for Cefuroxime Sodium is 56238-63-2. It is a Cephalosporin Antibiotic used in pharmaceutical antibacterial oral and parenteral formulations.

What therapeutic class does Cefuroxime Sodium belong to?

Cefuroxime Sodium is classified as a Cephalosporin Antibiotic. It is used in antibacterial oral and parenteral formulations and is an established API in both domestic Indian and international pharmaceutical markets.

What grades and purity specifications are available for Cefuroxime Sodium API?

Cefuroxime Sodium API is available in IP, BP, EP, and USP pharmacopeial grades with HPLC purity ≥98.0–102.0%, complete related substances profiling, and residual solvent analysis per ICH Q3C guidelines.

What is the minimum order quantity and lead time for Cefuroxime Sodium API?

Minimum order is 1 kg for sampling and 25 kg for commercial bulk supply. Standard lead time is 2–4 weeks from our Aurangabad, Maharashtra facility. Larger volumes may be available from existing stock.

Is DMF-grade documentation available for Cefuroxime Sodium API?

Yes, Swapnroop provides complete DMF-grade documentation for Cefuroxime Sodium API including Certificate of Analysis (CoA), MSDS, impurity profile, residual solvent certificate, and regulatory filing support for USFDA, EMA, and CDSCO submissions.

Cefuroxime Sodium API Bulk Supplier in Aurangabad, Maharashtra, India

Swapnroop Drugs and Pharmaceuticals is a trusted Cefuroxime Sodium API manufacturer and bulk supplier in Aurangabad, Maharashtra, serving pharmaceutical formulation companies across India and 25+ international markets. Our WHO-GMP certified facility provides consistent Cefuroxime Sodium API supply with full pharmacopeial compliance, competitive pricing, and complete regulatory documentation for domestic and export programs.

Cefuroxime Sodium API Exporter from India – Regulatory Filing Support

As a Cefuroxime Sodium API exporter from Maharashtra, India, Swapnroop supports pharmaceutical companies worldwide with DMF-grade documentation, Certificate of Analysis, MSDS, impurity profiles, and regulatory filing assistance for USFDA, EMA, and CDSCO submissions. Contact us for Cefuroxime Sodium API pricing, samples, and sourcing support.