Ganciclovir Sodium API Manufacturer in India

Swapnroop Pharma · WHO-GMP Certified · +91 87670 62101

Ganciclovir Sodium API Manufacturer and Bulk Supplier in India

Ganciclovir Sodium API (CAS No: 107910-75-8)

Antiviral Sodium Salt API for Cytomegalovirus and Injectable Anti-CMV Pharmaceutical Formulations

Ganciclovir Sodium API (CAS No. 107910-75-8) is the sodium salt form of Ganciclovir, an antiviral nucleoside analogue associated with cytomegalovirus (CMV) pharmaceutical applications. Ganciclovir belongs to the class of acyclic guanine nucleoside analogues and is associated with inhibition of viral DNA replication.

Following intracellular phosphorylation, Ganciclovir is converted to its pharmacologically active triphosphate form. Ganciclovir triphosphate inhibits viral DNA polymerase and interferes with viral DNA synthesis, thereby reducing replication of susceptible cytomegalovirus.

The sodium salt form is particularly relevant to parenteral and injectable pharmaceutical development. Pharmaceutical companies sourcing Ganciclovir Sodium API commonly evaluate assay, HPLC purity, sodium identity, related substances, process-related impurities, degradation products, residual solvents, water content, pH, solubility, and batch-to-batch consistency.

Salt-form identity and ionic composition are important quality considerations during Ganciclovir Sodium API qualification. Pharmaceutical buyers may evaluate sodium identification, chromatographic purity, related substances, water content, solution characteristics, and consistency of the impurity profile according to the approved product specification.

Ganciclovir Sodium is more suitable for aqueous pharmaceutical processing than the free Ganciclovir base because salt formation supports preparation of aqueous injectable formulations under controlled formulation conditions.

Swapnroop Drugs and Pharmaceuticals supplies Ganciclovir Sodium API for qualified pharmaceutical research, injectable formulation development, analytical, generic drug development, and regulated manufacturing requirements with product-specific quality documentation, pharmaceutical-grade packaging, and reliable supply-chain coordination.  Key Features

  • Ganciclovir Sodium API CAS No. 107910-75-8
  • Sodium salt form of Ganciclovir
  • Synthetic antiviral pharmaceutical active ingredient
  • Acyclic guanine nucleoside analogue sodium salt
  • Anti-cytomegalovirus pharmaceutical compound
  • Molecular formula C9H12N5NaO4
  • Molecular weight 277.21 g/mol
  • White to off-white powder
  • Controlled HPLC purity profile
  • Sodium identity testing
  • Salt-form confirmation
  • Related substances monitored according to approved specification
  • Process and degradation impurity monitoring
  • Solution characteristic evaluation
  • Residual solvents controlled according to applicable ICH Q3C requirements
  • Elemental impurities evaluated according to applicable ICH Q3D requirements
  • Pharmaceutical-grade packaging
  • COA and MSDS available as applicable
  • Bulk pharmaceutical supply and export coordination

Applications of Ganciclovir Sodium API

Ganciclovir Sodium API is primarily associated with:

  • Cytomegalovirus antiviral pharmaceutical development
  • Anti-CMV injectable pharmaceutical products
  • CMV retinitis pharmaceutical applications
  • Intravenous antiviral formulation development
  • Transplant-related CMV prevention product development
  • Injectable Ganciclovir product development
  • Antiviral nucleoside analogue research
  • Viral DNA polymerase inhibitor research
  • Generic injectable drug development
  • Hospital antiviral pharmaceutical products
  • Analytical and formulation research
  • Approved pharmaceutical manufacturing requirements

Ganciclovir Sodium is particularly associated with parenteral and intravenous Ganciclovir pharmaceutical products.

Ganciclovir Sodium API for Injectable Pharmaceutical Development

Ganciclovir Sodium is associated with injectable antiviral pharmaceutical development for cytomegalovirus-related applications.

Pharmaceutical formulation companies evaluating Ganciclovir Sodium API may review:

  • API assay
  • HPLC purity
  • Chemical identification
  • Sodium identification
  • Salt-form identity
  • Related substance profile
  • Process-related impurities
  • Degradation products
  • Residual solvents
  • Water content
  • Solution pH
  • Solution clarity
  • Solution color
  • Solubility characteristics
  • Formulation compatibility
  • Stability data
  • Batch-to-batch consistency

Product-specific API specifications should be evaluated according to the intended injectable dosage form, formulation process, target regulatory market, and approved pharmaceutical development requirements.

Ganciclovir Sodium API and CMV Pharmaceutical Applications

Ganciclovir Sodium is a pharmaceutical salt form associated with Ganciclovir-based antiviral products.

The antiviral activity is attributable to Ganciclovir following intracellular activation through phosphorylation. The resulting Ganciclovir triphosphate inhibits viral DNA polymerase and interferes with viral DNA synthesis.

Pharmaceutical companies developing Ganciclovir Sodium formulations may evaluate API purity, salt-form identity, impurity profile, solution characteristics, and formulation compatibility to support consistent drug-product manufacturing.

Ganciclovir and Ganciclovir Sodium

Ganciclovir and Ganciclovir Sodium should be treated as separate chemical material identities.

Ganciclovir free compound has CAS No. 82410-32-0, molecular formula C9H13N5O4, and molecular weight 255.23 g/mol.

Ganciclovir Sodium has CAS No. 107910-75-8, molecular formula C9H12N5NaO4, and molecular weight 277.21 g/mol.

Procurement, formulation, quality, and regulatory teams should confirm the exact required API or salt form before commercial sourcing.

Why Choose Swapnroop for Ganciclovir Sodium API?

Swapnroop Drugs and Pharmaceuticals supports qualified pharmaceutical and research customers with:

  • Reliable Ganciclovir Sodium API supply coordination
  • Product-specific specification support
  • COA and MSDS availability as applicable
  • Technical documentation coordination
  • Secure pharmaceutical-grade packaging
  • Bulk quantity supply support
  • Injectable formulation requirement coordination as applicable
  • Export documentation assistance
  • Global pharmaceutical supply coordination
  • Dedicated commercial enquiry support
  • Support for antiviral and injectable pharmaceutical development requirements

Packaging & Supply

Ganciclovir Sodium API is supplied in secure pharmaceutical-grade packaging selected according to product quantity, stability requirements, moisture protection requirements, and customer specifications.

Product-appropriate inner polyethylene liners and approved pharmaceutical-grade outer containers or HDPE drums may be used according to the supplied material specification.

Available packaging configurations may include:

  • 1 kg packaging
  • 5 kg packaging
  • 10 kg packaging
  • 25 kg packaging
  • Customer-specific packaging as applicable

Packaging configuration, MOQ, commercial quantity, formulation requirements, and shipment conditions are confirmed according to the approved product specification and customer enquiry.

Storage and Handling

Store Ganciclovir Sodium API in tightly closed and appropriately labeled containers under recommended controlled storage conditions.

Protect the material from excessive moisture, heat, direct light, and unsuitable environmental exposure.

Ganciclovir-related pharmaceutical materials require appropriate occupational handling controls. Handling should be performed by trained personnel using approved pharmaceutical material procedures, suitable containment practices, and applicable safety documentation.

Product-specific storage and handling requirements should be confirmed from the approved COA, SDS, specification, and stability documentation.

Ganciclovir Sodium API Manufacturer and Supplier in India

Swapnroop Drugs and Pharmaceuticals provides Ganciclovir Sodium API bulk supply and export support in India for qualified pharmaceutical manufacturers, injectable formulation developers, generic drug companies, antiviral pharmaceutical organizations, analytical laboratories, and pharmaceutical procurement customers.

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