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White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API
White Chemical Synthesis Levofloxacin API

White Chemical Synthesis Levofloxacin API

Price 4100 INR/ Kilograms

MOQ : 1000 Kilograms

White Chemical Synthesis Levofloxacin API Specification

  • EINECS No
  • 620-776-7
  • Smell
  • Odorless
  • Taste
  • Bitter
  • HS Code
  • 29419090
  • Melting Point
  • 220-225C
  • Loss on Drying
  • 0.5%
  • Solubility
  • Freely soluble in water and slightly soluble in chloroform, practically insoluble in ether
  • Storage
  • Store in tightly closed container, cool dry place, protect from light
  • Particle Size
  • D90 < 10 microns
  • Structural Formula
  • Available on request (standard levofloxacin structure)
  • Color
  • White
  • Boiling point
  • Not applicable (decomposes on heating)
  • Molecular Formula
  • C18H20FN3O4
  • Molecular Weight
  • 361.37 g/mol Grams (g)
  • Ph Level
  • 4.0-6.0 (5% solution)
  • Shelf Life
  • 36 months Years
  • Poisonous
  • Non-toxic if handled properly
  • Heavy Metal (%)
  • 0.002%
  • Medicine Name
  • Levofloxacin API
  • Chemical Name
  • Levofloxacin
  • CAS No
  • 100986-85-4
  • Type
  • Active Pharmaceutical Ingredient (API)
  • Grade
  • Pharmaceutical Grade
  • Usage
  • Used in the manufacture of antibiotic medicines for the treatment of bacterial infections
  • Purity(%)
  • 99%
  • Appearance
  • White Crystalline Powder
  • Physical Form
  • Powder
  • Residue on Ignition
  • 0.1%
  • Stability
  • Stable under recommended storage conditions
  • Packing Details
  • Double polyethylene bags packed in fiber drum
  • Identification Test
  • Meets USP/BP standards
  • Assay (By HPLC)
  • 99.5%
  • Moisture Content
  • 0.5%
  • Related Substances
  • 0.2%
  • Microbiology
  • Complies with Ph.Eur. standards (Total plate count 100 cfu/g)
  • Specific Rotation
  • +20 to +26
 

White Chemical Synthesis Levofloxacin API Trade Information

  • Minimum Order Quantity
  • 1000 Kilograms
  • FOB Port
  • mudara
  • Payment Terms
  • Paypal, Cash in Advance (CID), Letter of Credit at Sight (Sight L/C), Letter of Credit (L/C)
  • Supply Ability
  • 1000 Kilograms Per Day
  • Delivery Time
  • 5 Days
  • Packaging Details
  • 25kg Bag
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India
  • Certifications
  • coa
 

White Chemical Synthesis Levofloxacin API About

Levofloxacin, sold under the brand name Levaquin among others, is an antibiotic medication. It is used to treat a number of bacterial infections including acute bacterial sinusitis, pneumonia, H. pylori, urinary tract infections, chronic prostatitis, and some types of gastroenteritis.

Specification

Packaging Size

25kg

Manufacturer

NR

Composition

Levofloxacin API

Treatment

Levofloxacin, sold under the brand name Levaquin among others, is an antibiotic medication. It is us

Prescription/Non prescription

Prescription

Brand

NR

Form

Powder

Shelf life

1 Year



High Purity & Quality Assurance

Levofloxacin API is manufactured to stringent pharmaceutical-grade standards, meeting an assay of 99.5% and impurity thresholds of 0.2%. Its robust quality controls, including compliance with USP/BP and Ph.Eur. standards for identification and microbiology, ensure reliable performance in every batch. This results in a consistently pure and effective ingredient for antibiotic medicines.


Secure Packaging & Optimal Storage

To preserve its integrity, the API is packed in double polyethylene bags within sturdy fiber drums. This packaging minimizes contamination risks and shields the product from light and moisture. Recommended storage is in a tightly closed container in a cool, dry environment, allowing for a shelf life of up to 36 months without loss of potency or stability.


Versatile Application in Antibiotic Manufacturing

As a white crystalline powder, Levofloxacin API is designed for easy integration into various pharmaceutical formulations, especially antibiotics. Its solubility in water, low moisture content, and precise particle size facilitate smooth processing and uniform mixing, contributing to the effectiveness and quality of the final medicinal products.

FAQs of White Chemical Synthesis Levofloxacin API:


Q: How should Levofloxacin API be stored to maintain its quality?

A: Levofloxacin API should be stored in a tightly closed container, kept in a cool and dry place, and protected from light to ensure maximum stability and a shelf life of up to 36 months.

Q: What are the primary uses of this Levofloxacin API in pharmaceutical manufacturing?

A: This API is mainly used for manufacturing antibiotic medicines that target a wide range of bacterial infections, ensuring high efficacy due to its pharmaceutical-grade purity and compliance with global standards.

Q: When is Levofloxacin API considered compliant with international standards?

A: The API is compliant when it meets USP/BP identification standards, contains an assay of at least 99.5% (by HPLC), keeps related substances 0.2%, microbiology parameters (total plate count 100 cfu/g), and adheres to all specified physicochemical limits.

Q: Where is this Levofloxacin API manufactured and supplied from?

A: This Levofloxacin API is manufactured, distributed, and supplied by verified pharmaceutical companies in India, catering to global markets as a reliable source for high-quality antibiotic ingredients.

Q: What is the manufacturing process for ensuring product purity and consistency?

A: The manufacturing process involves advanced chemical synthesis and precise quality control procedures, including residue on ignition, moisture analysis, heavy metal testing, and HPLC assay, ensuring the final product is 99.5% pure and meets required pharmaceutical standards.

Q: How does the particle size and solubility of Levofloxacin API benefit formulation?

A: With a D90 particle size of less than 10 microns and high water solubility, the API ensures uniform dispersion in formulations, enhancing bioavailability and supporting consistent drug release profiles in finished products.

Q: What are the main benefits of using this specific Levofloxacin API?

A: Key benefits include high purity, compliance with major pharmacopeial standards, excellent physical properties, secure packaging, extended stability, and versatile application in developing effective antibiotic medicines.

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