VALSARTAN IP/BP/EP/USP

Name: VALSARTAN IP/BP/EP/USP
Brand: IPSUM LIFESCIENCES LLP
Price: 1800 INR
Availability: InStock

Price 1800 INR/ Kilograms

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VALSARTAN IP/BP/EP/USP Specification

Residue on Ignition
Not more than 0.1%

Place of Origin
India

Ph Level
Not less than 4.0 and not more than 8.0 (1% aqueous solution)

Storage
Store in a cool and dry place, away from light

Heavy Metal (%)
Not more than 0.001%

Particle Size
D90 < 10 micron

Assay
Not less than 99.0%

Molecular Weight
435.5 g/mol

Melting Point
105-110C

HS Code
29339900

Moisture (%)
Not more than 0.5%

Molecular Formula
C24H29N5O3

Loss on Drying
Not more than 0.5%

Other Names
VALSARTAN

CAS No
137862-53-4

Type
Pharmaceutical Raw Material

Grade
Pharmaceutical Grade

Usage
Used as an antihypertensive agent (treatment of high blood pressure)

Purity
99% (as per pharmacopoeial standards)

Appearance
White to off white powder

Application
Used in the formulation of anti-hypertensive medications

Raw Material
Active Pharmaceutical Ingredient (API)

Smell
Odorless

Color
White to off white

Form
Powder

About VALSARTAN IP/BP/EP/USP

Valsartan is an angiotensin II receptor antagonist used primarily for the treatment of hypertension (high blood pressure) and various cardiovascular conditions. Its chemical structure is characterized by the molecular formula C24H29N5O3 and a molecular weight of approximately 435.5 g/mol. By selectively blocking the angiotensin II receptor subtype 1 (AT1), primarily found in vascular smooth muscle and adrenal glands, valsartan inhibits the vasoconstrictor and aldosterone-secreting effects of angiotensin II.

Comprehensive Quality and Compliance

Valsartan IP/BP/EP/USP is produced by qualified manufacturers in India using synthetic methods. The product complies fully with all major pharmacopeial standards (IP/BP/EP/USP), ensuring that it meets stringent purity, impurity, microbial, and endotoxin limits. Detailed regulatory documentation (DMF/EDMF) is submitted, and every batch is tested against validated reference standards, guaranteeing consistent quality and compliance.

Flexible Packaging and Ready Supply

To maintain pharmaceutical-grade integrity, valsartan is supplied in HDPE drums with double PE bag liners. Custom packaging can be arranged as per client requirements. With abundant ready stock and bulk supply capability, pharmaceutical manufacturers and traders worldwide benefit from reliable, on-time shipmentshipped as a non-hazardous product under ambient conditions from India.

Safe Storage and Handling

Valsartan should be stored in a cool, dry environment away from light to maintain its efficacy throughout its 36-month shelf life. The product is non-hazardous and can be transported at room temperature. Quality-focused processes ensure it remains free from BSE/TSE risk and complies with all key safety parameters, making it a trusted choice for antihypertensive medication production.

FAQs of VALSARTAN IP/BP/EP/USP:

Q: How should valsartan IP/BP/EP/USP be stored and transported to maintain quality?

A: Valsartan should be kept in a cool, dry place, protected from light, and in tightly closed HDPE drums with double PE bags. It is chemically stable during shipment at ambient temperature and classified as non-hazardous for transport.

Q: What regulatory and pharmacopoeial standards does valsartan comply with?

A: This product conforms to IP/BP/EP/USP requirements. It also has DMF and EDMF documentation submitted, ensuring adherence to international pharmaceutical regulations and standards for active pharmaceutical ingredients.

Q: When is valsartan typically used in the pharmaceutical industry?

A: Valsartan is primarily utilized as an active pharmaceutical ingredient (API) in the formulation of anti-hypertensive medications, playing a central role in drugs prescribed for the management of high blood pressure.

Q: Where is valsartan IP/BP/EP/USP manufactured and exported from?

A: Valsartan IP/BP/EP/USP is manufactured and shipped from India, with export capabilities supporting clients worldwide through established supply chains and ready stock in bulk quantities.

Q: What is the process used for manufacturing valsartan, and how does it ensure contaminant-free product?

A: Valsartan is synthetic in origin and produced using stringent pharmaceutical processes. Each batch is ensured to be free from BSE/TSE risk, with comprehensive impurity, microbial, and endotoxin limits in full compliance with international standards.

Q: What are the key benefits of choosing valsartan from this supplier?

A: This valsartan is distinguished by its high purity (99%), pharmacopoeial compliance, secure packaging, flexible supply options, and reliable regulatory support, providing pharmaceutical manufacturers with a trusted source for antihypertensive drug production.

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