SB19102

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04 Looking for 496775-62-3 / Eltrombopag API manufacturers, exporters & distributors?

PharmaCompass offers a list of Eltrombopag 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 Eltrombopag manufacturer or Eltrombopag supplier for your needs.

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

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

API | Excipient name

Eltrombopag

Synonyms

496775-62-3, Revolade, Promacta, Eltrombopag (olamine), Unii-4u07f515lg, Sb-497115-gr

Cas Number

496775-62-3

Unique Ingredient Identifier (UNII)

4U07F515LG

About Eltrombopag

Eltrombopag Olamine is the orally active ethanolamine salt of eltrombopag, a small-molecule, nonpeptide thrombopoietin receptor agonist with megakaryopoiesis-stimulating activity. Eltrombopag binds to and stimulates the transmembrane domain of the platelet thrombopoietin receptor (TPO-R or CD110), a member of the hematopoietin receptor superfamily. Activation of TPO-R leads to the proliferation and differentiation of cells in the megakaryocytic lineage and an increase in platelet production.

SB19102 Manufacturers

A SB19102 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SB19102, including repackagers and relabelers. The FDA regulates SB19102 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SB19102 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 SB19102 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

SB19102 Suppliers

A SB19102 supplier is an individual or a company that provides SB19102 active pharmaceutical ingredient (API) or SB19102 finished formulations upon request. The SB19102 suppliers may include SB19102 API manufacturers, exporters, distributors and traders.

click here to find a list of SB19102 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

SB19102 KDMF

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

Pharmaceutical companies submit a SB19102 Drug Master File in Korea (SB19102 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of SB19102. The MFDS reviews the SB19102 KDMF as part of the drug registration process and uses the information provided in the SB19102 KDMF to evaluate the safety and efficacy of the drug.

After submitting a SB19102 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 SB19102 API can apply through the Korea Drug Master File (KDMF).

click here to find a list of SB19102 suppliers with KDMF on PharmaCompass.

SB19102 Manufacturers | Traders | Suppliers

We have 4 companies offering SB19102

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

56 API Suppliers

22 USDMF

3 JDMF

8 EU WC

4 KDMF

15 NDC API

34 Listed Suppliers

$ API Reference Price

DEVELOPMENTS

62 Drugs in Development

INTERMEDIATES

21 Intermediate Suppliers

FINISHED DOSAGE FORMULATIONS

91 FDF Dossiers

33 FDA Orange Book

10 Europe

4 Canada

16 Australia

2 South Africa

26 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET;ORAL - EQ 100MG ACID **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

TABLET;ORAL - EQ 12.5MG ACID

TABLET;ORAL - EQ 25MG ACID

TABLET;ORAL - EQ 50MG ACID

TABLET;ORAL - EQ 75MG ACID

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EXCIPIENTS BY APPLICATIONS

47 Fillers, Diluents & Binders

46 Coating Systems & Additives

TABLET;ORAL - EQ 100MG ACID Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons