EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI GERMANY GmbH Frankfurt am Main DE
02 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
03 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
01 3Nadolol
01 1France
02 2India
01 3Valid
Certificate Number : R1-CEP 2010-058 - Rev 02
Status : Valid
Issue Date : 2021-12-10
Type : Chemical
Substance Number : 1789
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Certificate Number : CEP 2017-209 - Rev 02
Status : Valid
Issue Date : 2024-07-16
Type : Chemical
Substance Number : 1789
Certificate Number : CEP 2009-372 - Rev 04
Status : Valid
Issue Date : 2024-07-22
Type : Chemical
Substance Number : 1789
A Nadolol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nadolol, including repackagers and relabelers. The FDA regulates Nadolol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nadolol 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 Nadolol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nadolol supplier is an individual or a company that provides Nadolol active pharmaceutical ingredient (API) or Nadolol finished formulations upon request. The Nadolol suppliers may include Nadolol API manufacturers, exporters, distributors and traders.
click here to find a list of Nadolol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nadolol CEP of the European Pharmacopoeia monograph is often referred to as a Nadolol Certificate of Suitability (COS). The purpose of a Nadolol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nadolol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nadolol to their clients by showing that a Nadolol CEP has been issued for it. The manufacturer submits a Nadolol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nadolol CEP holder for the record. Additionally, the data presented in the Nadolol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nadolol DMF.
A Nadolol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nadolol 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 Nadolol suppliers with CEP (COS) on PharmaCompass.
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