01 1IPCA LABORATORIES LIMITED Mumbai IN
02 1MANKIND PHARMA LIMITED New Delhi IN
01 2Propranolol hydrochloride
01 2India
01 2Valid
Certificate Number : CEP 2002-026 - Rev 06
Status : Valid
Issue Date : 2023-12-06
Type : Chemical
Substance Number : 568
Certificate Number : R0-CEP 2021-104 - Rev 00
Status : Valid
Issue Date : 2023-08-30
Type : Chemical
Substance Number : 568
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PharmaCompass offers a list of Propranolol Hydrochloride 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 Propranolol Hydrochloride manufacturer or Propranolol Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Propranolol Hydrochloride manufacturer or Propranolol Hydrochloride supplier.
PharmaCompass also assists you with knowing the Propranolol Hydrochloride API Price utilized in the formulation of products. Propranolol Hydrochloride API Price is not always fixed or binding as the Propranolol Hydrochloride Price is obtained through a variety of data sources. The Propranolol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Scandrug manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Scandrug, including repackagers and relabelers. The FDA regulates Scandrug manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Scandrug 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 Scandrug manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Scandrug supplier is an individual or a company that provides Scandrug active pharmaceutical ingredient (API) or Scandrug finished formulations upon request. The Scandrug suppliers may include Scandrug API manufacturers, exporters, distributors and traders.
click here to find a list of Scandrug suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Scandrug CEP of the European Pharmacopoeia monograph is often referred to as a Scandrug Certificate of Suitability (COS). The purpose of a Scandrug CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Scandrug EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Scandrug to their clients by showing that a Scandrug CEP has been issued for it. The manufacturer submits a Scandrug CEP (COS) as part of the market authorization procedure, and it takes on the role of a Scandrug CEP holder for the record. Additionally, the data presented in the Scandrug CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Scandrug DMF.
A Scandrug CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Scandrug CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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