About Benfotiamine API
| Packaging Size |
25 kg
|
| Form |
Powder
|
| Country of Origin |
Made in India
|
| Minimum Order Quantity |
10 Kg
|
We are manufacturer and exporter of Benfotiamine API
It is used for the treatment and prevention of diabetic nephropathy and diabetes mellitus, type 2. In the last few years we have established ourselves as one of the most prominent organizations engaged in offering Benfotiamine . It is a synthetic version of thiamine, essential for many of the body
Pharmaceutical Grade QualityBenfotiamine API is produced under strict quality controls, including an assay of 98.5% by HPLC and a purity exceeding 99%. All batches comply with ICH guidelines for residual solvents and heavy metal limits, ensuring excellent safety and efficacy. Our product undergoes thorough testing for microbial and endotoxin levels to guarantee patient safety.
Safe and Reliable HandlingThis active ingredient is non-poisonous and odorless, making it safe to handle during manufacturing. Its stable crystalline form is slightly bitter in taste and designed for easy formulation. Packaged securely in double polythene bags within HDPE drums, it maintains its quality during storage and transport.
Therapeutic Application and UsageBenfotiamine API is widely used in treating diabetic neuropathy and other neurological disorders. Its slightly water-soluble nature and favorable pH allow for formulation versatility in various pharmaceutical preparations, supporting innovative therapies for nerve-related conditions.
FAQs of Benfotiamine API:
Q: How is Benfotiamine API typically used in pharmaceutical formulations?
A: Benfotiamine API is primarily used as the key active ingredient in medications targeting diabetic neuropathy and neurological disorders. Its excellent purity, stability, and pharmaceutical grade ensure reliable performance in tablets, capsules, and other dosage forms.
Q: What benefits does Benfotiamine API offer over regular thiamine derivatives?
A: Benfotiamine exhibits superior bioavailability and stability compared to standard thiamine. This leads to enhanced absorption and efficacy in treating nerve-related conditions, making it a preferred choice for formulating advanced neurological therapies.
Q: Where is Benfotiamine API manufactured and supplied from?
A: This API is manufactured, exported, and supplied from India by reputable producers experienced in pharmaceutical ingredients. The product adheres to international standards, ensuring consistent quality for global distribution.
Q: What is the recommended storage condition for Benfotiamine API?
A: Benfotiamine API should be stored below 25C, protected from moisture and light, in its original packaging. This preserves its crystalline integrity and chemical stability for its full 36-month shelf life.
Q: How does the packaging process ensure the quality of Benfotiamine API?
A: The API is packed in double polythene bags placed inside high-grade HDPE drums, available in sizes of 5kg, 10kg, and 25kg. This robust packaging shields the product from environmental contaminants and maintains its purity during storage and transit.
Q: What quality specifications comply with international guidelines for Benfotiamine API?
A: The API conforms to strict ICH guidelines for residual solvents; has related substances 1.0%; a water content of 0.20%; and meets all criteria for microbial and endotoxin limits, ensuring it is suitable for pharmaceutical use globally.