DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1AZICO BIOPHORE INDIA PRIVATE LIMITED Hyderabad IN
05 1GEDEON RICHTER PLC Budapest HU
06 1HETERO DRUGS LIMITED Hyderabad IN
07 1IPCA LABORATORIES LIMITED Mumbai IN
08 1IPCA Laboratories Limited Mumbai IN
09 1MSN LIFE SCIENCES PRIVATE LIMITED Bhiknoor Village IN
10 1NAKODA CHEMICALS LIMITED Hyderabad IN
11 1ORCHEV PHARMA PRIVATE LIMITED Rajkot IN
12 1PHALANX LABS PRIVATE LIMITED Hyderabad IN
13 1RAKSHIT PHARMACEUTICALS LIMITED Anakapalli IN
14 2SMS PHARMACEUTICALS LIMITED Hyderabad IN
15 1SULESHVARI PHARMA Ankleshwar IN
16 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R1-CEP 2009-161 - Rev 01
Status : Valid
Issue Date : 2023-05-31
Type : Chemical
Substance Number : 1012
38
PharmaCompass offers a list of Famotidine 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 Famotidine manufacturer or Famotidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Famotidine manufacturer or Famotidine supplier.
PharmaCompass also assists you with knowing the Famotidine API Price utilized in the formulation of products. Famotidine API Price is not always fixed or binding as the Famotidine Price is obtained through a variety of data sources. The Famotidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Durater manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Durater, including repackagers and relabelers. The FDA regulates Durater manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Durater 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 Durater manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Durater supplier is an individual or a company that provides Durater active pharmaceutical ingredient (API) or Durater finished formulations upon request. The Durater suppliers may include Durater API manufacturers, exporters, distributors and traders.
click here to find a list of Durater suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Durater CEP of the European Pharmacopoeia monograph is often referred to as a Durater Certificate of Suitability (COS). The purpose of a Durater CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Durater EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Durater to their clients by showing that a Durater CEP has been issued for it. The manufacturer submits a Durater CEP (COS) as part of the market authorization procedure, and it takes on the role of a Durater CEP holder for the record. Additionally, the data presented in the Durater CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Durater DMF.
A Durater CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Durater 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 Durater suppliers with CEP (COS) on PharmaCompass.
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