Clarithromycin API Manufacturer India

High-Quality Active Pharmaceutical Ingredient for Anti-Infective and Antiviral Formulations

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Clarithromycin API Manufacturer India

Product Specifications

Product Name: Clarithromycin API
CAS Number: 29110-48-3
Category: Active Pharmaceutical Ingredient
Grade: 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% โ€“ 102.0%
Loss on DryingNMT 1.0%
Residue on IgnitionNMT 0.2%
Heavy MetalsNMT 10 ppm
pH (1% Solution)2.0 โ€“ 4.0
Individual Impurityโ‰ค 0.5%
Total Impuritiesโ‰ค 1.5%

Clarithromycin API (CAS No: 29110-48-3 )

High-Quality Active Pharmaceutical Ingredient for Anti-Infective and Antiviral Formulations

Clarithromycin API is positioned for companies seeking a dependable active pharmaceutical ingredient source backed by organized quality systems and scalable supply support.

Our manufacturing and supply approach for Clarithromycin emphasizes dependable commercial support, efficient order management, and pharma-focused service for long-term buyers.

Clarithromycin is commonly assessed on quality consistency, handling profile, packaging suitability, and documentation readiness before it is approved for downstream formulation use.

Key Features

  • Documentation support aligned with customer qualification needs
  • Batch-to-batch consistency focused for commercial supply
  • Bulk packaging options designed for safe storage and dispatch
  • Supply planning suited to domestic and export demand

Applications

  • Suitable for formulation development and scale-up studies
  • Used by pharmaceutical buyers seeking consistent raw material supply and documentation coordination
  • Can support commercial procurement, validation batches, and routine production programs
  • Supports manufacturers working on anti-infective, antiviral, and infection-management dosage forms.

Why Choose Us

  • Consistent commercial communication and responsive quotation support
  • Focus on repeatability, supply continuity, and practical business support
  • Bulk packaging and logistics support for domestic and export dispatch
  • Structured documentation assistance for buyer evaluation

Packaging & Supply

We offer Clarithromycin API in pharma-oriented packaging formats including HDPE or fiber drum options with inner protection layers, helping maintain handling quality during storage, shipping, and routine supply movement.

Get Bulk Quote

Clarithromycin API Bulk Supplier in India

For companies evaluating Clarithromycin API manufacturer options in India, this page offers a clear overview of the product profile, quality approach, and supply readiness.

Clarithromycin API Manufacturer for Commercial Sourcing

Our team works with buyers who need Clarithromycin API backed by practical documentation support, organized batch handling, and efficient supply communication for ongoing business.

Frequently Asked Questions about Clarithromycin

What is the CAS number for Clarithromycin API?

The CAS number for Clarithromycin API is 29110-48-3. Please verify the exact salt or hydrate form you require as different forms carry distinct CAS numbers.

What purity and grade is Clarithromycin API available in?

Clarithromycin API is available in IP / BP / EP / USP pharmacopeial grades, manufactured under WHO-GMP certified conditions with full impurity profiling per ICH Q3A and pharmacopeial identification testing (IR, HPLC).

What is the MOQ and lead time for Clarithromycin?

Minimum order is 1 kg for R&D sampling and 25 kg for commercial bulk supply. Standard lead time is 2-4 weeks from our Aurangabad, Maharashtra facility. Expedited supply available for urgent requirements.

Is DMF documentation available for Clarithromycin API?

Yes, Swapnroop provides full DMF-grade documentation for Clarithromycin API including CoA, MSDS, impurity report, stability data, and complete regulatory dossier support for USFDA, EMA, and CDSCO submissions.