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List of Drug Master Files (JDMF) for MolPort-001-792-509 Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Japan (PMDA). Original Data : PMDA Database

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01 Asahi Kasei Finechem Co., Ltd. (1)

02 Yamasa Soy Sauce Co., Ltd. (1)

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01 Cytarabine ocfosfate "Yamasa" (1)

02 Japanese Pharmacopoeia cytarabine (production only) (1)

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01 Japan (2)

URL Supplier Web Content
217MF10811
3-3-23 Nakanoshima, Kita-ku, Osaka-...
2007-08-01
2005-11-01
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URL Supplier Web Content
218MF10475
2-10-1 Shinseicho, Choshi City, Chi...
2009-01-28
2006-05-15
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Looking for 147-94-4 / Cytarabine API manufacturers, exporters & distributors?

Cytarabine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Cytarabine

Synonyms

147-94-4, Ara-c, Cytosine arabinoside, Arabinocytidine, Aracytin, Depocyt

Cas Number

147-94-4

Unique Ingredient Identifier (UNII)

04079A1RDZ

About Cytarabine

A pyrimidine nucleoside analog that is used mainly in the treatment of leukemia, especially acute non-lymphoblastic leukemia. Cytarabine is an antimetabolite antineoplastic agent that inhibits the synthesis of DNA. Its actions are specific for the S phase of the cell cycle. It also has antiviral and immunosuppressant properties. (From Martindale, The Extra Pharmacopoeia, 30th ed, p472)

MolPort-001-792-509 Manufacturers

A MolPort-001-792-509 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-792-509, including repackagers and relabelers. The FDA regulates MolPort-001-792-509 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-792-509 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 MolPort-001-792-509 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-792-509 Suppliers

A MolPort-001-792-509 supplier is an individual or a company that provides MolPort-001-792-509 active pharmaceutical ingredient (API) or MolPort-001-792-509 finished formulations upon request. The MolPort-001-792-509 suppliers may include MolPort-001-792-509 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-792-509 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-792-509 JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The MolPort-001-792-509 Drug Master File in Japan (MolPort-001-792-509 JDMF) empowers MolPort-001-792-509 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the MolPort-001-792-509 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-001-792-509 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of MolPort-001-792-509 suppliers with JDMF on PharmaCompass.

MolPort-001-792-509 Manufacturers | Traders | Suppliers

MolPort-001-792-509 Manufacturers, Traders, Suppliers 1
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We have 2 companies offering MolPort-001-792-509

Get in contact with the supplier of your choice:

  1. Asahi Kasei Finechem
  2. Yamasa Corporation
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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