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List of Drug Master Files (JDMF) for Tox21_300515 Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Japan (PMDA). Original Data : PMDA Database

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01 Biovet JSC (1)

02 ERCROS S. A. (1)

03 HEC PHARM CO. ,LTD (1)

04 Ningxia Qiyuan Pharmaceutical Co. , Ltd. (2)

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01 Erythromycin (1)

02 Erythromycin Chioshianeito (1)

03 erythromycin (3)

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01 Bulgaria (1)

02 China (3)

03 Spain (1)

URL Supplier Web Content
217MF10893
39 Petar Rakov Street 4550 Peshtera...
2010-03-09
2005-11-07
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218MF10942
Paseo del Deleite, s/n 28300 Aranju...
2006-11-24
2006-11-24
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231MF10067
No. 62 Binjiang Road, Yidu, Hubei P...
2019-03-11
2019-03-11
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228MF10123
No. 1 Qiyuan Street, Wangyuan Indus...
2016-07-06
2016-07-06
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227MF10101
No. 1 Qiyuan Street, Wangyuan Indus...
2015-04-09
2015-04-09
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Looking for 114-07-8 / Erythromycin API manufacturers, exporters & distributors?

Erythromycin manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Erythromycin

Synonyms

114-07-8, Erythromycin a, E-mycin, Ilotycin, Abomacetin, Erymax

Cas Number

114-07-8

Unique Ingredient Identifier (UNII)

63937KV33D

About Erythromycin

A bacteriostatic antibiotic macrolide produced by Streptomyces erythreus. Erythromycin A is considered its major active component. In sensitive organisms, it inhibits protein synthesis by binding to 50S ribosomal subunits. This binding process inhibits peptidyl transferase activity and interferes with translocation of amino acids during translation and assembly of proteins.

Tox21_300515 Manufacturers

A Tox21_300515 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300515, including repackagers and relabelers. The FDA regulates Tox21_300515 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300515 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_300515 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Tox21_300515 Suppliers

A Tox21_300515 supplier is an individual or a company that provides Tox21_300515 active pharmaceutical ingredient (API) or Tox21_300515 finished formulations upon request. The Tox21_300515 suppliers may include Tox21_300515 API manufacturers, exporters, distributors and traders.

click here to find a list of Tox21_300515 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Tox21_300515 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 Tox21_300515 Drug Master File in Japan (Tox21_300515 JDMF) empowers Tox21_300515 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 Tox21_300515 JDMF during the approval evaluation for pharmaceutical products. At the time of Tox21_300515 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 Tox21_300515 suppliers with JDMF on PharmaCompass.

Tox21_300515 Manufacturers | Traders | Suppliers

Tox21_300515 Manufacturers, Traders, Suppliers 1
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We have 4 companies offering Tox21_300515

Get in contact with the supplier of your choice:

  1. Biovet AD
  2. Ercros
  3. HEC Pharm
  4. Ningxia Qiyuan 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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