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PharmaCompass
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

CEP 2014-321 - Rev 02
Valid
Chemical
2024-01-25
2570
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01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Desloratadine

Certificate Number : CEP 2014-321 - Rev 02

Status : Valid

Issue Date : 2024-01-25

Type : Chemical

Substance Number : 2570

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Desloratadine Manufacturers

A Desloratadine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desloratadine, including repackagers and relabelers. The FDA regulates Desloratadine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desloratadine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Desloratadine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Desloratadine Suppliers

A Desloratadine supplier is an individual or a company that provides Desloratadine active pharmaceutical ingredient (API) or Desloratadine finished formulations upon request. The Desloratadine suppliers may include Desloratadine API manufacturers, exporters, distributors and traders.

click here to find a list of Desloratadine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Desloratadine CEP

A Desloratadine CEP of the European Pharmacopoeia monograph is often referred to as a Desloratadine Certificate of Suitability (COS). The purpose of a Desloratadine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Desloratadine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Desloratadine to their clients by showing that a Desloratadine CEP has been issued for it. The manufacturer submits a Desloratadine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Desloratadine CEP holder for the record. Additionally, the data presented in the Desloratadine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Desloratadine DMF.

A Desloratadine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Desloratadine CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of Desloratadine suppliers with CEP (COS) on PharmaCompass.

Desloratadine Manufacturers | Traders | Suppliers

Desloratadine Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.