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 Nevofam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nevofam, including repackagers and relabelers. The FDA regulates Nevofam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nevofam 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 Nevofam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nevofam supplier is an individual or a company that provides Nevofam active pharmaceutical ingredient (API) or Nevofam finished formulations upon request. The Nevofam suppliers may include Nevofam API manufacturers, exporters, distributors and traders.
click here to find a list of Nevofam suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nevofam CEP of the European Pharmacopoeia monograph is often referred to as a Nevofam Certificate of Suitability (COS). The purpose of a Nevofam CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nevofam EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nevofam to their clients by showing that a Nevofam CEP has been issued for it. The manufacturer submits a Nevofam CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nevofam CEP holder for the record. Additionally, the data presented in the Nevofam CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nevofam DMF.
A Nevofam CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nevofam 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 Nevofam suppliers with CEP (COS) on PharmaCompass.
We have 14 companies offering Nevofam
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