01 1CHROMO LABORATORIES INDIA PRIVATE LIMITED Pashamylaram IN
02 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
03 1SYMED LABS LIMITED Hyderabad IN
01 3Levocetirizine dihydrochloride
01 1Gabon
02 2India
01 3Valid
Levocetirizine Dihydrochloride
Certificate Number : CEP 2023-225 - Rev 00
Status : Valid
Issue Date : 2024-07-09
Type : Chemical
Substance Number : 3115
Levocetirizine Dihydrochloride
Certificate Number : CEP 2024-050 - Rev 00
Status : Valid
Issue Date : 2024-08-26
Type : Chemical
Substance Number : 3115
Levocetirizine Dihydrochloride
Certificate Number : CEP 2024-171 - Rev 00
Status : Valid
Issue Date : 2024-12-12
Type : Chemical
Substance Number : 3115
A Levocetirizine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levocetirizine Dihydrochloride, including repackagers and relabelers. The FDA regulates Levocetirizine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levocetirizine Dihydrochloride 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 Levocetirizine Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levocetirizine Dihydrochloride supplier is an individual or a company that provides Levocetirizine Dihydrochloride active pharmaceutical ingredient (API) or Levocetirizine Dihydrochloride finished formulations upon request. The Levocetirizine Dihydrochloride suppliers may include Levocetirizine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Levocetirizine Dihydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levocetirizine Dihydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Levocetirizine Dihydrochloride Certificate of Suitability (COS). The purpose of a Levocetirizine Dihydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Levocetirizine Dihydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Levocetirizine Dihydrochloride to their clients by showing that a Levocetirizine Dihydrochloride CEP has been issued for it. The manufacturer submits a Levocetirizine Dihydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Levocetirizine Dihydrochloride CEP holder for the record. Additionally, the data presented in the Levocetirizine Dihydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Levocetirizine Dihydrochloride DMF.
A Levocetirizine Dihydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Levocetirizine Dihydrochloride 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 Levocetirizine Dihydrochloride suppliers with CEP (COS) on PharmaCompass.
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