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Sulfadiazine BP USP
Sulfadiazine BP USP

Sulfadiazine BP USP

Price 100 INR/ Kilograms

MOQ : As per order Kilograms

Sulfadiazine BP USP Specification

  • Type
  • Antibiotic Raw Material
  • Main Ingredient
  • Sulfadiazine
  • Form
  • Powder
  • Variety
  • Pharmaceutical Grade
  • Suitable For
  • Adults
  • Grade
  • BP/USP
  • Color
  • White
  • Moisture (%)
  • Not More Than 0.5%
  • Ash %
  • Not More Than 0.1%
  • Application
  • Pharmaceutical Preparation
  • Dosage
  • As Prescribed
  • Efficacy
  • Bacterial Infection Control
  • Function
  • Antibacterial
  • Disease prevention
  • Treatment of bacterial infections
  • Shelf Life
  • 5 Years
  • Molecular Weight
  • 250.28 g/mol
  • Solubility
  • Slightly soluble in water
  • Melting Point
  • 250C
  • Storage Condition
  • Store in a cool, dry place, tightly closed
  • Purity
  • 99%
  • Molecular Formula
  • C10H10N4O2S
 

Sulfadiazine BP USP Trade Information

  • Supply Ability
  • 1000 Kilograms Per Day
  • Delivery Time
  • 1-3 Days
 

About Sulfadiazine BP USP



Sulfadiazine BP USP pharmaceutical grade powderpristine in quality and radiant with 99% purityis ending soon for our current promotion. A champion among antibiotic raw materials, Sulfadiazine is proven for bacterial infection control and is ideal for pharmaceutical preparation. Buy or try now to experience efficacy, supported by a five-year shelf life and BP/USP certified standards. Carefully packaged and exported from India, it remains stable with a moisture content not exceeding 0.5%. Secure your pristine supply before this opportunity ends!

Sulfadiazine BP USP: Application & Advantages

Sulfadiazine BP USP is a champion ingredient in pharmaceutical manufacturing, primarily used to control bacterial infections in adults. Its application method involves precise blending into antibiotic formulations, ensuring consistent efficacy. The advantage lies in its purity and stability, contributing to radiant product outcomes while meeting strict industry standards. Its slightly soluble nature enhances compatibility with other pharmaceutical agents, making it suitable for various dosage forms and treatment regimens.


Sample, Supply & Certifications for Sulfadiazine BP USP

Sample availability allows buyers to verify quality before purchase, with list price details provided upon inquiry. Once dispatched, orders are tracked until safe arrival, ensuring transparency and reliability. Backed by robust supply ability, the product is promptly distributed by certified exporter, importer, supplier, and trader in India. Trusted certifications guarantee compliance with BP/USP grade and pharmaceutical standards, assuring buyers of product authenticity and consistent excellence.


FAQs of Sulfadiazine BP USP:


Q: How should Sulfadiazine BP USP be stored for maximum shelf life?

A: Sulfadiazine BP USP should be stored in a cool, dry place with the container tightly closed to maintain its pristine quality and ensure its five-year shelf life.

Q: What is the main benefit of using Sulfadiazine BP USP in pharmaceutical applications?

A: The main benefit is its highly pure antibacterial function, enabling effective bacterial infection control in pharmaceutical preparation for adult patients.

Q: When is Sulfadiazine BP USP supply typically dispatched and how long does it take to arrive?

A: Once the order is confirmed and processed, Sulfadiazine BP USP is dispatched promptly, and arrival time may vary based on the destination and shipping method chosen.

Q: Where can I obtain certification details for Sulfadiazine BP USP?

A: Certification details are available through the supplier, who provides proof of BP/USP grade and compliance with pharmaceutical standards upon request.

Q: What process is followed to ensure product purity and quality?

A: Every batch of Sulfadiazine BP USP undergoes rigorous testing for purity (99%), moisture, and ash content, ensuring compliance with BP/USP specifications and consistent quality.

Q: How is Sulfadiazine BP USP applied in pharmaceutical formulations?

A: Sulfadiazine BP USP is carefully blended into formulations as a raw material, under controlled conditions, based on prescribed dosage and specific pharmaceutical requirements.

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