DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 1SYMED LABS LIMITED Hyderabad IN
01 2Tizanidine hydrochloride
01 2India
01 2Valid
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R0-CEP 2020-281 - Rev 00
Status : Valid
Issue Date : 2023-07-05
Type : Chemical
Substance Number : 2578
Certificate Number : R0-CEP 2022-256 - Rev 00
Status : Valid
Issue Date : 2023-01-05
Type : Chemical
Substance Number : 2578
A Tizanidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tizanidine Hydrochloride, including repackagers and relabelers. The FDA regulates Tizanidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tizanidine Hydrochloride 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 Tizanidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tizanidine Hydrochloride supplier is an individual or a company that provides Tizanidine Hydrochloride active pharmaceutical ingredient (API) or Tizanidine Hydrochloride finished formulations upon request. The Tizanidine Hydrochloride suppliers may include Tizanidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Tizanidine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tizanidine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Tizanidine Hydrochloride Certificate of Suitability (COS). The purpose of a Tizanidine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tizanidine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tizanidine Hydrochloride to their clients by showing that a Tizanidine Hydrochloride CEP has been issued for it. The manufacturer submits a Tizanidine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tizanidine Hydrochloride CEP holder for the record. Additionally, the data presented in the Tizanidine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tizanidine Hydrochloride DMF.
A Tizanidine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tizanidine Hydrochloride 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 Tizanidine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
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