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Ofloxacin BP-USP-EP

Ofloxacin BP-USP-EP
Ofloxacin BP-USP-EP

Ofloxacin BP-USP-EP Specification

  • Solubility
  • Slightly soluble in water-soluble in acetic acid,slightly soluble in methanol
  • Heavy Metal (%)
  • 0.001
  • Loss on Drying
  • 0.2
  • Molecular Formula
  • C18H20FN3O4
  • Molecular Weight
  • 361.373 g/mol
  • Storage
  • Dry Place
  • Shelf Life
  • 5 Years
  • Medicine Name
  • Ofloxacin
  • Chemical Name
  • Ofloxacine; Floxin; Tarivid; Oxaldin
  • CAS No
  • 82419-36-1
  • Type
  • Antibiotic and Antimicrobial Agents
  • Grade
  • Medicine Grade
  • Usage
  • Pharmaceutical
  • Purity(%)
  • 98.5%-105.5%
  • Appearance
  • White or yellowish crystalline powder
  • Physical Form
  • Powder
 

Ofloxacin BP-USP-EP Trade Information

  • Minimum Order Quantity
  • 50 Kilograms
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
 

About Ofloxacin BP-USP-EP

It is used to treat certain bacterial infections in many different parts of the body. It may also be used for other problems as determined by your doctor. Ofloxacin may mask or delay the symptoms of syphilis. It is not effective against syphilis infections. Ofloxacin belongs to the class of drugs known as fluoroquinolone antibiotics. It works by killing bacteria or preventing their growth. However, this medicine will not work for colds, flu, or other virus infections. 



Effective Broad-Spectrum Antibiotic

Ofloxacin BP-USP-EP plays a vital role in the pharmaceutical industry as an effective antibacterial and antimicrobial compound. Its broad spectrum allows it to combat a range of bacterial infections, making it a preferred choice in formulating various medicinal products.


Superior Purity and Quality Standards

Maintaining a purity range of 98.5% to 105.5% and minimal heavy metal presence, Ofloxacin BP-USP-EP adheres rigorously to international quality benchmarks such as BP, USP, and EP standards, ensuring patient safety and efficacy in end-use pharmaceuticals.


Long Shelf Life with Stable Storage

With a shelf life of five years, Ofloxacin retains its medicinal properties over extended periods. For optimal stability, it should be stored in a cool, dry place away from direct sunlight, preserving its efficacy for pharmaceutical manufacturing.

FAQs of Ofloxacin BP-USP-EP:


Q: How is Ofloxacin BP-USP-EP typically used in pharmaceutical applications?

A: Ofloxacin BP-USP-EP is primarily utilized as an active pharmaceutical ingredient in the formulation of antibiotics that treat various bacterial infections. Its broad-spectrum efficacy makes it suitable for inclusion in capsules, tablets, and oral suspensions.

Q: What are the storage recommendations for Ofloxacin BP-USP-EP powder?

A: To preserve its potency and stability, Ofloxacin BP-USP-EP should be kept in a dry place, away from moisture, heat, and direct sunlight. Proper storage extends its shelf life and ensures consistent performance in pharmaceutical manufacturing.

Q: When does Ofloxacin BP-USP-EP expire, and what is its shelf life?

A: The shelf life of Ofloxacin BP-USP-EP is five years from the date of manufacture, provided that it is stored under appropriate conditions as recommended by the manufacturer.

Q: Where is Ofloxacin BP-USP-EP produced and supplied from?

A: Ofloxacin BP-USP-EP is manufactured and exported from India, ensuring compliance with global pharmaceutical standards. It is supplied worldwide by certified manufacturers, exporters, and suppliers based in India.

Q: What are the benefits of choosing Ofloxacin BP-USP-EP with a purity of 98.5%-105.5%?

A: Selecting Ofloxacin BP-USP-EP with high purity ensures effective antimicrobial action, minimal impurities, and consistent quality, which is crucial for producing safe and reliable medicinal products.

Q: How is Ofloxacin BP-USP-EP processed to ensure quality standards are met?

A: Ofloxacin BP-USP-EP undergoes rigorous quality testing and is produced following BP, USP, and EP guidelines. This process ensures high purity, precise chemical composition, and strict control of heavy metal content.

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