With Virupaksha, you get a quality product with on-time delivery.
01 1VIRUPAKSHA ORGANICS LIMITED Hyderabad IN
02 1AMI LIFESCIENCES PRIVATE LIMITED Karakhadi IN
03 1Grunenthal GmbH Aachen DE
04 1SYMED LABS LIMITED Hyderabad IN
05 1YICHANG HUMANWELL PHARMACEUTICAL CO., LTD. Yichang CN
01 4Tapentadol hydrochloride
02 1Tapentadol hydrochloride, Form-A
01 1China
02 1Germany
03 3India
01 5Valid
With Virupaksha, you get a quality product with on-time delivery.
With Virupaksha, you get a quality product with on-time delivery.
Certificate Number : CEP 2023-142 - Rev 00
Status : Valid
Issue Date : 2024-10-31
Type : Chemical
Substance Number : 3035
AMI Lifesciences is Driven by Chemistry. Powered by People.
AMI Lifesciences is Driven by Chemistry. Powered by People.
Certificate Number : R0-CEP 2021-290 - Rev 00
Status : Valid
Issue Date : 2022-11-24
Type : Chemical
Substance Number : 3035
Certificate Number : R0-CEP 2021-390 - Rev 00
Status : Valid
Issue Date : 2022-10-03
Type : Chemical
Substance Number : 3035
Tapentadol Hydrochloride, Form-A
Certificate Number : CEP 2022-252 - Rev 00
Status : Valid
Issue Date : 2024-02-27
Type : Chemical
Substance Number : 3035
Certificate Number : CEP 2024-119 - Rev 00
Status : Valid
Issue Date : 2025-02-28
Type : Chemical
Substance Number : 3035
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PharmaCompass offers a list of Tapentadol 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 Tapentadol manufacturer or Tapentadol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tapentadol manufacturer or Tapentadol supplier.
PharmaCompass also assists you with knowing the Tapentadol API Price utilized in the formulation of products. Tapentadol API Price is not always fixed or binding as the Tapentadol Price is obtained through a variety of data sources. The Tapentadol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nucynta ER manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nucynta ER, including repackagers and relabelers. The FDA regulates Nucynta ER manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nucynta ER API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Nucynta ER supplier is an individual or a company that provides Nucynta ER active pharmaceutical ingredient (API) or Nucynta ER finished formulations upon request. The Nucynta ER suppliers may include Nucynta ER API manufacturers, exporters, distributors and traders.
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A Nucynta ER CEP of the European Pharmacopoeia monograph is often referred to as a Nucynta ER Certificate of Suitability (COS). The purpose of a Nucynta ER CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nucynta ER EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nucynta ER to their clients by showing that a Nucynta ER CEP has been issued for it. The manufacturer submits a Nucynta ER CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nucynta ER CEP holder for the record. Additionally, the data presented in the Nucynta ER CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nucynta ER DMF.
A Nucynta ER CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nucynta ER CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Nucynta ER suppliers with CEP (COS) on PharmaCompass.
We have 5 companies offering Nucynta ER
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