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Amlodipine Besilate

Name: Amlodipine Besilate
Brand: FORTUNE HEALTHCARE PRODUCTS PVT LTD

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MOQ : 1 Box

Amlodipine Besilate Specification

Storage
Store protected from moisture and light, at room temperature

Heavy Metal (%)
Not more than 0.001%

Ph Level
4.0 6.0 (in water suspension)

Assay
Not less than 99.0% and not more than 101.0% (on dried basis)

Residue on Ignition
Not more than 0.1%

Moisture (%)
Not more than 1.0%

Place of Origin
India

Molecular Formula
C20H25ClN2O5C6H6O3S

Molecular Weight
567.05 g/mol

EINECS No
None

Particle Size
D90 75 m (micronized powder)

Loss on Drying
Not more than 0.5%

HS Code
29349900

Other Names
Amlodipine 2.5mg, 5mg, 10mg; Amlodipine Besylate

Type
Active Pharmaceutical Ingredient (API)

Grade
Pharmaceutical Grade

Purity
99% (HPLC)

Appearance
White or almost white powder

Application
Pharmaceuticals, Cardiovascular drugs, Antihypertensive agent

Raw Material
Yes

Smell
Odorless

Color
White

Form
Powder

Amlodipine Besilate Trade Information

Minimum Order Quantity
1 Box

Supply Ability
100 Boxes Per Week

Delivery Time
1 Week

About Amlodipine Besilate

Amlodipine Besilate

We have gained immense appreciation among our clients for manufacturing and exporting a highly effective assortment of Amlodipine Besilate. These drugs are effective in treating high blood pressure. Also, angina that results from coronary spasm and exertion can be cured and treated using our offered Amlodipine Besilate. All these drugs are medically approved in the industry for their accurate composition.The drugs offered by us are highly acclaimed in market as these do not cause any kind of side effect on the body.

Highly Pure and Stable API

Amlodipine Besilate stands out with outstanding purity (99% by HPLC) and is supplied as a finely micronized powder (D90 75 m), enabling consistent drug formulation. Its stability is maintained by protecting it from moisture and light at room temperature, ensuring long shelf-life for pharmaceutical applications.

Wide Pharmaceutical Applications

Primarily used in the production of antihypertensive agents, Amlodipine Besilate is essential for cardiovascular drugs. Its reliable chemical structure facilitates its application as a raw material by manufacturers looking to develop effective therapies for blood pressure and related heart conditions.

FAQs of Amlodipine Besilate:

Q: How should Amlodipine Besilate powder be stored for optimal stability?

A: Amlodipine Besilate should be stored protected from moisture and light and kept at room temperature. Proper storage is crucial for maintaining its purity and effectiveness as an active pharmaceutical ingredient.

Q: What is the primary usage of Amlodipine Besilate in pharmaceuticals?

A: Amlodipine Besilate is primarily used as a raw material in the production of antihypertensive and cardiovascular drugs. Its main function is to contribute to the formulation of medications intended to manage high blood pressure and heart-related disorders.

Q: When should a pharmaceutical manufacturer consider using micronized Amlodipine Besilate?

A: Manufacturers should opt for micronized Amlodipine Besilate when a uniform particle size is necessary for consistent blending and absorption in tablet production, or when high purity and controlled physical properties are required for sensitive formulations.

Q: Where is Amlodipine Besilate typically produced and exported from?

A: Amlodipine Besilate is often manufactured, supplied, and exported from India, a key hub for pharmaceutical-grade active ingredients globally.

Q: What are the benefits of using pharmaceutical-grade Amlodipine Besilate with high assay and low impurities?

A: Using pharmaceutical-grade Amlodipine Besilate (assay not less than 99.0%, low moisture and heavy metal content) ensures product efficacy, safety, and regulatory compliance for finished drug products, minimizing the risk of contamination and variability in formulations.

Q: How is the quality of Amlodipine Besilate guaranteed during the manufacturing process?

A: Quality is ensured through rigorous analytical methods including HPLC for purity, tests for moisture, loss on drying, heavy metals, and strict adherence to defined assay parameters and pharmaceutical standards.

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