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List of NDC API details of Tox21_202591 Active Pharmaceutical Ingredient listed on PharmaCompass.com

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Flag Finland
Digital Content Digital Content
MERCAPTOPURINE
POWDER (1kg/kg)
BULK INGREDIENT
12780-0299
2001-01-15
2024-12-31
Flag India
Digital Content Digital Content
Mercaptopurine
POWDER (1kg/kg)
BULK INGREDIENT
15308-0712
1983-01-01
2024-12-31
Flag U.S.A
Digital Content Digital Content
URL Supplier Web Content
Mercaptopurine
POWDER (1g/g)
BULK INGREDIENT FOR ...
62991-2899
2011-12-19
2024-12-31
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MERCAPTOPURINE MONOHYDRATE
POWDER (1kg/kg)
BULK INGREDIENT
66122-0016
2019-12-13
2024-12-31
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Looking for 50-44-2 / Mercaptopurine API manufacturers, exporters & distributors?

Mercaptopurine manufacturers, exporters & distributors 1

77

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

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

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

API | Excipient name

Mercaptopurine

Synonyms

6-mercaptopurine, 50-44-2, Purinethol, Mercapurin, 6-thiopurine, Leukerin

Cas Number

50-44-2

Unique Ingredient Identifier (UNII)

PKK6MUZ20G

About Mercaptopurine

An antimetabolite antineoplastic agent with immunosuppressant properties. It interferes with nucleic acid synthesis by inhibiting purine metabolism and is used, usually in combination with other drugs, in the treatment of or in remission maintenance programs for leukemia.

Tox21_202591 Manufacturers

A Tox21_202591 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202591, including repackagers and relabelers. The FDA regulates Tox21_202591 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202591 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 Tox21_202591 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Tox21_202591 Suppliers

A Tox21_202591 supplier is an individual or a company that provides Tox21_202591 active pharmaceutical ingredient (API) or Tox21_202591 finished formulations upon request. The Tox21_202591 suppliers may include Tox21_202591 API manufacturers, exporters, distributors and traders.

click here to find a list of Tox21_202591 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Tox21_202591 NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Tox21_202591 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Tox21_202591 API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Tox21_202591 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Tox21_202591 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tox21_202591 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Tox21_202591 suppliers with NDC on PharmaCompass.

Tox21_202591 Manufacturers | Traders | Suppliers

Tox21_202591 Manufacturers, Traders, Suppliers 1
98

We have 4 companies offering Tox21_202591

Get in contact with the supplier of your choice:

  1. Fermion Oy
  2. Aarti Pharmalabs
  3. Letco Medical
  4. Zhejiang Cheng Yi Pharmaceutical Co., Ltd
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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