Pyrantel Pamoate USP API with DMF

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Product Details:

Solubility Practically insoluble in water, freely soluble in chloroform and methanol
Smell Odorless
Storage Store in a tightly closed container, protected from light and moisture at room temperature
EINECS No 244-837-1
Poisonous Non-poisonous, if used as directed
Shelf Life 36 months
Boiling point Not applicable (decomposes before boiling)
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Pyrantel Pamoate USP API with DMF Price And Quantity

Minimum Order Quantity 100 Kilograms

Pyrantel Pamoate USP API with DMF Product Specifications

Color Yellow
Heavy Metal (%) NMT 0.001%
Medicine Name Pyrantel Pamoate USP API with DMF
Purity(%) >=99%
Molecular Formula C34H30N2O6S
CAS No 22204-24-6
Ph Level 6.5 - 7.5 (1% solution in water)
HS Code 29349900
Structural Formula Available on request
Molecular Weight 594.68 g/mol
Melting Point > 200C (decomposes)
Loss on Drying NMT 0.5%
Particle Size D90 < 40 microns
Usage Anthelmintic/Used for the treatment of intestinal worm infections
Poisonous Non-poisonous, if used as directed
Type Active Pharmaceutical Ingredient (API)
Physical Form Solid
Grade USP
Shelf Life 36 months
Chemical Name (E)-1,4,5,6-tetrahydro-1-methyl-2-(2-thienylcarbonyl)pyrimidine-4,4-pamoate
Boiling point Not applicable (decomposes before boiling)
Solubility Practically insoluble in water, freely soluble in chloroform and methanol
Smell Odorless
Appearance Fine Yellow Powder
EINECS No 244-837-1
Storage Store in a tightly closed container, protected from light and moisture at room temperature

Assay (On dried basis) >=99.0% (by HPLC)
End Application Pharmaceutical formulations (tablets, suspensions, chewable tablets, oral solutions)
Impurities Within USP limits
Identification Complies with USP Standards (IR, HPLC)
Packaging HDPE drums with double polyethylene liners, 25 kg net
Microbial Limits Total aerobic microbial count: NMT 1000 CFU/g, Total combined yeasts and molds: NMT 100 CFU/g
Manufacturer Certification GMP, WHO-GMP, ISO 9001:2015
Residual Solvents Complies with USP requirements
Controls Particle size test, Bulk density, Tap density, Individual impurity test
Stability Stable under recommended storage conditions
DMF Status Available (Drug Master File Registered)

Pyrantel Pamoate USP API with DMF Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 7 Days

Product Description

Pyrantel Pamoate USP API with DMF is a best-seller, acclaimed for its sterling quality and gilt-edged compliance with USP standards. Offered at a reduced price, it is a first-class, non-poisonous active pharmaceutical ingredient for anthelmintic use in treating intestinal worm infections. Manufactured under strict GMP and WHO-GMP guidelines, it boasts a purity of 99% and outstanding stability for 36 months. The API meets all regulatory specifications-DMF registered, impurities within USP limits, and comprehensive testing for bulk density, individual impurity, and particle size, ensuring top-tier pharmaceutical reliability.

Advantages & Features of Pyrantel Pamoate USP API with DMF

Pyrantel Pamoate USP API with DMF offers distinct advantages, such as its exceptional assay of 99.0% and compliance with all USP standards. The fine yellow powder is practically insoluble in water, yet freely soluble in chloroform and methanol. Special features include robust particle size control, stringent bulk and tap density testing, and comprehensive impurity assessments. Its stability under recommended storage conditions and non-poisonous profile set it apart for high-quality pharmaceutical formulations.

Packaging Details, Payment Terms & Sample Availability

This first-class API is securely packed in HDPE drums with double polyethylene liners, 25 kg net, ensuring a safe drop-off. Express shipping and global distribution are available. Flexible payment terms are offered for convenience, and product samples can be arranged on request, with a nominal charge. Whether you're a distributor or manufacturer, our streamlined logistics ensure prompt delivery and reliability for every order.

FAQ's of Pyrantel Pamoate USP API with DMF:

Q: How is the quality of Pyrantel Pamoate USP API with DMF assured?

A: The API fully complies with USP standards, features a DMF registration, and undergoes comprehensive tests, including assay (99.0%), impurity analysis, and microbial limits, ensuring sterling, first-class quality.

Q: What pharmaceutical applications is Pyrantel Pamoate USP API suitable for?

A: It is used in manufacturing tablets, chewable tablets, suspensions, and oral solutions for the treatment of intestinal worm infections.

Q: Where is Pyrantel Pamoate USP API manufactured and supplied from?

A: The API is manufactured and supplied in India by GMP, WHO-GMP, and ISO 9001:2015 certified facilities, catering to distributors, exporters, importers, and wholesalers globally.

Q: What are the packaging and shipping options for this API?

A: Pyrantel Pamoate USP API is packaged in 25 kg HDPE drums with double polyethylene liners for secure drop-off and express shipping to various locations.

Q: Is a product sample of Pyrantel Pamoate USP API available for evaluation?

A: Yes, samples can be provided for quality evaluation upon request, with a small sample charge applied.

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