Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
01 1MANKIND PHARMA LIMITED New Delhi IN
02 1IPCA LABORATORIES LIMITED Mumbai IN
01 2Propranolol hydrochloride
01 2India
01 2Valid
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
Certificate Number : R0-CEP 2021-104 - Rev 00
Status : Valid
Issue Date : 2023-08-30
Type : Chemical
Substance Number : 568
Certificate Number : CEP 2002-026 - Rev 06
Status : Valid
Issue Date : 2023-12-06
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 Nedis manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nedis, including repackagers and relabelers. The FDA regulates Nedis manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nedis 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 Nedis manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nedis supplier is an individual or a company that provides Nedis active pharmaceutical ingredient (API) or Nedis finished formulations upon request. The Nedis suppliers may include Nedis API manufacturers, exporters, distributors and traders.
click here to find a list of Nedis suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nedis CEP of the European Pharmacopoeia monograph is often referred to as a Nedis Certificate of Suitability (COS). The purpose of a Nedis CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nedis EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nedis to their clients by showing that a Nedis CEP has been issued for it. The manufacturer submits a Nedis CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nedis CEP holder for the record. Additionally, the data presented in the Nedis CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nedis DMF.
A Nedis CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nedis 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 Nedis suppliers with CEP (COS) on PharmaCompass.
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