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List of Tox21_202522 NDC API suppliers/manufacturers & exporters

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01 American Pacific Corporation (2)

02 DARMERICA, LLC (1)

03 Hetero Labs Limited (1)

04 Sionc Pharmaceutical Private Limited (1)

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01 MELPHALAN (1)

02 Melphalan (3)

03 Melphalan, sieved (1)

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01 India (2)

02 U.S.A (3)

URL Supplier Web Content
Melphalan, sieved
POWDER (1kg/kg)
BULK INGREDIENT
50683-0520
2017-03-01
2024-12-31
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Melphalan
POWDER (1kg/kg)
BULK INGREDIENT
50683-0385
2002-02-01
2024-12-31
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Melphalan
POWDER (5g/5g)
BULK INGREDIENT
71052-158
2020-08-17
2024-12-31
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Melphalan
POWDER (1kg/kg)
BULK INGREDIENT
68554-0076
1982-01-01
2023-12-31
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MELPHALAN
POWDER (1kg/kg)
BULK INGREDIENT
76055-0021
2019-12-31
2024-12-31
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Looking for 148-82-3 / Melphalan API manufacturers, exporters & distributors?

Melphalan manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Melphalan

Synonyms

148-82-3, Alkeran, Melfalan, L-pam, Phenylalanine mustard, L-sarcolysine

Cas Number

148-82-3

Unique Ingredient Identifier (UNII)

Q41OR9510P

About Melphalan

An alkylating nitrogen mustard that is used as an antineoplastic in the form of the levo isomer - MELPHALAN, the racemic mixture - MERPHALAN, and the dextro isomer - MEDPHALAN; toxic to bone marrow, but little vesicant action; potential carcinogen.

Tox21_202522 Manufacturers

A Tox21_202522 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202522, including repackagers and relabelers. The FDA regulates Tox21_202522 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202522 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_202522 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Tox21_202522 Suppliers

A Tox21_202522 supplier is an individual or a company that provides Tox21_202522 active pharmaceutical ingredient (API) or Tox21_202522 finished formulations upon request. The Tox21_202522 suppliers may include Tox21_202522 API manufacturers, exporters, distributors and traders.

click here to find a list of Tox21_202522 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Tox21_202522 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_202522 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Tox21_202522 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_202522 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_202522 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tox21_202522 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Tox21_202522 suppliers with NDC on PharmaCompass.

Tox21_202522 Manufacturers | Traders | Suppliers

Tox21_202522 Manufacturers, Traders, Suppliers 1
52

We have 4 companies offering Tox21_202522

Get in contact with the supplier of your choice:

  1. American Pacific Corporation
  2. Darmerica
  3. Hetero Drugs
  4. Sionc Pharmaceuticals
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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