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01 1STEROID S. p. A.

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Testosterone Enanthate

Registration Number : 304MF10082

Registrant's Address : Viale Spagna, 156 Cologno Monzese (MI) - ITALY

Initial Date of Registration : 2022-06-01

Latest Date of Registration : 2022-06-01

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Looking for 315-37-7 / Testosterone Enanthate API manufacturers, exporters & distributors?

Testosterone Enanthate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Testosterone Enanthate

Synonyms

315-37-7, Testosterone heptanoate, Androtardyl, Testosterone enantate, Testosterone heptylate, Atlatest

Cas Number

315-37-7

Unique Ingredient Identifier (UNII)

7Z6522T8N9

About Testosterone Enanthate

Testosterone Enanthate is a long-acting intramuscular form of the androgen testosterone. Testosterone inhibits gonadotropin secretion from the pituitary gland and ablates estrogen production in the ovaries, thereby decreasing endogenous estrogen levels. In addition, this agent promotes the maintenance of male sex characteristics and is indicated for testosterone replacement in hypogonadal males, delayed puberty, and metastatic mammary cancer. (NCI04)

Testosteron Depot-Rotexmedica Manufacturers

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

Testosteron Depot-Rotexmedica Suppliers

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

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

Testosteron Depot-Rotexmedica 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 Testosteron Depot-Rotexmedica Drug Master File in Japan (Testosteron Depot-Rotexmedica JDMF) empowers Testosteron Depot-Rotexmedica 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 Testosteron Depot-Rotexmedica JDMF during the approval evaluation for pharmaceutical products. At the time of Testosteron Depot-Rotexmedica 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 Testosteron Depot-Rotexmedica suppliers with JDMF on PharmaCompass.

Testosteron Depot-Rotexmedica Manufacturers | Traders | Suppliers

Testosteron Depot-Rotexmedica Manufacturers, Traders, Suppliers 1
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We have 1 companies offering Testosteron Depot-Rotexmedica

Get in contact with the supplier of your choice:

  1. Steroid SpA
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.