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List of NDC API details of MolPort-001-783-551 Active Pharmaceutical Ingredient listed on PharmaCompass.com

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Thiotepa
POWDER (1kg/kg)
BULK INGREDIENT
50683-0465
2020-01-13
2024-12-31
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Thiotepa
POWDER (1kg/kg)
BULK INGREDIENT
54893-0045
2016-03-31
2024-12-31
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Thiotepa
POWDER (0.1kg/.1kg)
BULK INGREDIENT
70225-1104
2017-12-09
2024-12-31
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Heraeus Precious Metals GmbH & Co. ...

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Thiotepa
POWDER (1g/g)
BULK INGREDIENT
54875-0004
2013-05-02
2024-12-31
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  • POWDER;INTRACAVITARY, INTRAVENOUS, INTRAVESICAL - 100MG/VIAL
  • POWDER;INTRACAVITARY, INTRAVENOUS, INTRAVESICAL - 15MG/VIAL

Looking for 52-24-4 / Thiotepa API manufacturers, exporters & distributors?

Thiotepa manufacturers, exporters & distributors 1

24

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

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

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

API | Excipient name

Thiotepa

Synonyms

Thio-tepa, 52-24-4, Triethylenethiophosphoramide, Thioplex, Thiophosphamide, Tiofosfamid

Cas Number

52-24-4

Unique Ingredient Identifier (UNII)

905Z5W3GKH

About Thiotepa

A very toxic alkylating antineoplastic agent also used as an insect sterilant. It causes skin, gastrointestinal, CNS, and bone marrow damage. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), thiotepa may reasonably be anticipated to be a carcinogen (Merck Index, 11th ed).

MolPort-001-783-551 Manufacturers

A MolPort-001-783-551 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-783-551, including repackagers and relabelers. The FDA regulates MolPort-001-783-551 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-783-551 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-001-783-551 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-783-551 Suppliers

A MolPort-001-783-551 supplier is an individual or a company that provides MolPort-001-783-551 active pharmaceutical ingredient (API) or MolPort-001-783-551 finished formulations upon request. The MolPort-001-783-551 suppliers may include MolPort-001-783-551 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-783-551 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-783-551 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 MolPort-001-783-551 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for MolPort-001-783-551 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 MolPort-001-783-551 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 MolPort-001-783-551 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MolPort-001-783-551 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of MolPort-001-783-551 suppliers with NDC on PharmaCompass.

MolPort-001-783-551 Manufacturers | Traders | Suppliers

MolPort-001-783-551 Manufacturers, Traders, Suppliers 1
52

We have 3 companies offering MolPort-001-783-551

Get in contact with the supplier of your choice:

  1. American Pacific Corporation
  2. MSN Laboratories
  3. Natco Pharma
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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