DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR

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04 Looking for 100643-71-8 / Desloratadine API manufacturers, exporters & distributors?

PharmaCompass offers a list of Desloratadine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Desloratadine manufacturer or Desloratadine supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desloratadine manufacturer or Desloratadine supplier.

PharmaCompass also assists you with knowing the Desloratadine API Price utilized in the formulation of products. Desloratadine API Price is not always fixed or binding as the Desloratadine Price is obtained through a variety of data sources. The Desloratadine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Desloratadine

Synonyms

100643-71-8, Clarinex, Descarboethoxyloratadine, Desloratidine, Neoclarityn, Aerius

Cas Number

100643-71-8

Unique Ingredient Identifier (UNII)

FVF865388R

About Desloratadine

Desloratadine is a long-acting piperidine derivate with selective H1 antihistaminergic and non-sedating properties. Desloratadine diminishes the typical histaminergic effects on H1-receptors in bronchial smooth muscle, capillaries and gastrointestinal smooth muscle, including vasodilation, bronchoconstriction, increased vascular permeability, pain, itching and spasmodic contractions of gastrointestinal smooth muscle. Desloratadine is used to provide symptomatic relieve of allergic symptoms.

DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR Manufacturers

A DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR, including repackagers and relabelers. The FDA regulates DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR 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; PSEUDOEPHEDRINE SULFATE 24 HOUR manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR Suppliers

A DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR supplier is an individual or a company that provides DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR active pharmaceutical ingredient (API) or DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR finished formulations upon request. The DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR suppliers may include DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR API manufacturers, exporters, distributors and traders.

click here to find a list of DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR Drug Master File in Korea (DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR. The MFDS reviews the DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR KDMF as part of the drug registration process and uses the information provided in the DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR KDMF to evaluate the safety and efficacy of the drug.

After submitting a DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR API can apply through the Korea Drug Master File (KDMF).

click here to find a list of DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR suppliers with KDMF on PharmaCompass.

DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR Manufacturers | Traders | Suppliers

We have 3 companies offering DESLORATADINE; PSEUDOEPHEDRINE SULFATE 24 HOUR

Get in contact with the supplier of your choice:

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.

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CHEMISTRY

Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

57 API Suppliers

16 USDMF

14 CEP/COS

3 JDMF

23 EU WC

4 KDMF

9 NDC API

36 Listed Suppliers

$ API Reference Price

DEVELOPMENTS

3 Drugs in Development

INTERMEDIATES

13 Intermediate Suppliers

FINISHED DOSAGE FORMULATIONS

289 FDF Dossiers

24 FDA Orange Book

153 Europe

6 Canada

50 South Africa

56 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET;ORAL - 5MG

SOLUTION;ORAL - 0.5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

TABLET, EXTENDED RELEASE;ORAL - 2.5MG;120MG

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SOLUTION;ORAL - 0.5MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons