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Product Details:
- EINECS No No data available
- Heavy Metal (%) 20 ppm
- Melting Point 207-209C
- Particle Size Micronized grade available
- Boiling point Not applicable (decomposes)
- Loss on Drying 0.5%
- Smell Odorless
X
Glimepiride IP/BP Price And Quantity
- 100 Kilograms
Glimepiride IP/BP Product Specifications
- 99%
- Glimepiride
- No data available
- 0.5%
- Odorless
- White to off-white crystalline powder
- Micronized grade available
- 207-209C
- Solid
- 20 ppm
- Glimepiride IP/BP
- Not applicable (decomposes)
- Store in a cool, dry place, away from light
- 29420090
- No data available
- As shown in image
- Not applicable / not specified
- Used as an oral antidiabetic drug (sulfonylurea class)
- C24H34N4O5S
- White to off-white
- Pharmaceutical Raw Material / API
- Practically insoluble in water, soluble in dimethylformamide, slightly soluble in methanol
- 490.62 g/mol
- 93479-97-1
- No (when used as prescribed)
- 5 years
- IP/BP (Indian / British Pharmacopoeia)
- Total impurities not more than 1.0%
- Antidiabetic Agent
- 98.0% to 102.0%
- Infrared absorption spectroscopy complies with the standard
- HDPE drum or customized packaging
- Not more than 0.1%
- Pharmacopoeial grade, available with DMF/TDMF
Glimepiride IP/BP Trade Information
- Cash in Advance (CID)
- 5000 Kilograms Per Month
- 10 Days
- All India
Product Description
Glimepiride IP/BP is used for diabetes type 2 patients for controlling high blood sugar level. It acts as an insulin secretagogue and works by stimulating the release of insulin by beta cells of pancreas. It is processed using quality approved chemicals under the supervision of our adroit professionals with the aid of sophisticated methodology. Furthermore, we provide this Glimepiride IP/BP at very nominal rates.
Exceptional Quality and Compliance
Glimepiride IP/BP is meticulously tested for regulatory standards, including assay, identification by infrared spectroscopy, residue on ignition, and related substances. Each batch undergoes comprehensive analysis ensuring a purity of 99% and impurity levels well below accepted thresholds. This results in a consistently high-quality pharmaceutical raw material suitable for critical applications in antidiabetic drug formulations.
Therapeutic Application
This product is used widely as an oral antidiabetic agent within the sulfonylurea class. Its mechanism assists in controlling blood sugar levels, aiding patients with type 2 diabetes. The raw material is suitable for use by pharmaceutical manufacturers and institutions aiming to produce effective antidiabetes medications that meet international standards.
Packaging, Storage, and Shelf Life
Glimepiride IP/BP is securely packaged in HDPE drums or can be provided according to your specific requirements. The compound must be stored in a cool, dry place, away from light, ensuring its stability over a five-year shelf life. Micronized grades are also available, accommodating specialized pharmaceutical production needs.
FAQ's of Glimepiride IP/BP:
Q: How is Glimepiride IP/BP identified for quality assurance?
A: Glimepiride IP/BP is identified using infrared absorption spectroscopy, which ensures that the compound complies with pharmacopoeial standards before being released for pharmaceutical use.Q: What are the key benefits of using Glimepiride IP/BP as a pharmaceutical raw material?
A: Glimepiride IP/BP offers high purity, meets stringent pharmacopeial parameters, and provides reliable therapeutic action as an oral antidiabetic agent. It supports consistent drug formulation and regulatory compliance.Q: When should Glimepiride IP/BP be stored and handled under specific conditions?
A: To maintain stability and efficacy, Glimepiride IP/BP should be stored in a cool, dry place, away from light. Adhering to these conditions ensures the product retains its defined shelf life of five years.Q: Where is Glimepiride IP/BP typically sourced and supplied from?
A: It is manufactured and exported from India, available globally to pharmaceutical companies as both a standard and customized order to fit various regulatory and industrial requirements.Q: What is the process for verifying the purity and safety of Glimepiride IP/BP?
A: Each batch undergoes rigorous testing, including evaluation of assay (98.0% - 102.0%), impurity levels (not more than 1.0%), residue on ignition (0.1%), and ensures heavy metal content does not exceed 20 ppm for patient safety.Q: How is Glimepiride IP/BP used in antidiabetic drug formulations?
A: Manufacturers use Glimepiride IP/BP as the active pharmaceutical ingredient in oral medications intended for managing type 2 diabetes, leveraging its proven sulfonylurea class efficacy.Tell us about your requirement
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