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Pyrantel Pamoate USP API with DMF
Pyrantel Pamoate USP API with DMF
Pyrantel Pamoate USP API with DMF
Pyrantel Pamoate USP API with DMF
Pyrantel Pamoate USP API with DMF
Pyrantel Pamoate USP API with DMF
Pyrantel Pamoate USP API with DMF
Pyrantel Pamoate USP API with DMF
Pyrantel Pamoate USP API with DMF
Pyrantel Pamoate USP API with DMF
Pyrantel Pamoate USP API with DMF
Pyrantel Pamoate USP API with DMF

Pyrantel Pamoate USP API with DMF

Price 3200 INR/ Kilograms

MOQ : 100 Kilograms

Pyrantel Pamoate USP API with DMF Specification

  • Melting Point
  • > 200C (decomposes)
  • Storage
  • Store in a tightly closed container, protected from light and moisture at room temperature
  • Poisonous
  • Non-poisonous, if used as directed
  • Molecular Weight
  • 594.68 g/mol
  • Shelf Life
  • 36 months
  • Boiling point
  • Not applicable (decomposes before boiling)
  • Solubility
  • Practically insoluble in water, freely soluble in chloroform and methanol
  • Smell
  • Odorless
  • Heavy Metal (%)
  • NMT 0.001%
  • Particle Size
  • D90 < 40 microns
  • Color
  • Yellow
  • EINECS No
  • 244-837-1
  • Ph Level
  • 6.5 - 7.5 (1% solution in water)
  • Molecular Formula
  • C34H30N2O6S
  • Loss on Drying
  • NMT 0.5%
  • Structural Formula
  • Available on request
  • HS Code
  • 29349900
  • Medicine Name
  • Pyrantel Pamoate USP API with DMF
  • Chemical Name
  • (E)-1,4,5,6-tetrahydro-1-methyl-2-(2-thienylcarbonyl)pyrimidine-4,4-pamoate
  • CAS No
  • 22204-24-6
  • Type
  • Active Pharmaceutical Ingredient (API)
  • Grade
  • USP
  • Usage
  • Anthelmintic/Used for the treatment of intestinal worm infections
  • Purity(%)
  • >=99%
  • Appearance
  • Fine Yellow Powder
  • Physical Form
  • Solid
  • 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
  • DMF Status
  • Available (Drug Master File Registered)
  • Packaging
  • HDPE drums with double polyethylene liners, 25 kg net
  • Stability
  • Stable under recommended storage conditions
  • Impurities
  • Within USP limits
  • Assay (On dried basis)
  • >=99.0% (by HPLC)
  • End Application
  • Pharmaceutical formulations (tablets, suspensions, chewable tablets, oral solutions)
  • Identification
  • Complies with USP Standards (IR, HPLC)
  • Controls
  • Particle size test, Bulk density, Tap density, Individual impurity test
  • Residual Solvents
  • Complies with USP requirements
 

Pyrantel Pamoate USP API with DMF Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • Payment Terms
  • Cash on Delivery (COD), Cash in Advance (CID), Cheque, Days after Acceptance (DA), Letter of Credit at Sight (Sight L/C), Telegraphic Transfer (T/T), Letter of Credit (L/C)
  • Supply Ability
  • 1000 Kilograms Per Month
  • Delivery Time
  • 7 Days
  • Sample Available
  • Yes
  • Sample Policy
  • Contact us for information regarding our sample policy
  • Main Export Market(s)
  • Asia, Australia, South America, Africa
  • Main Domestic Market
  • All India, South India, Central India, West India, North India, East India, Gujarat
 

About Pyrantel Pamoate USP API with DMF



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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