Neuland Laboratories- A dedicated 100% API provider.
01 1NEULAND LABORATORIES LIMITED Hyderabad IN
02 1AARTI DRUGS LIMITED Mumbai IN
03 1AUROBINDO PHARMA LIMITED Hyderabad IN
04 1BAYER AG Leverkusen DE
05 1CIPLA LIMITED Mumbai IN
06 2DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
07 1HANGZHOU HUADONG MEDICINE GROUP ZHEJIANG HUAYI PHARMACEUTICAL CO., LTD. Yiwu CN
08 1INDOCO REMEDIES LIMITED Mumbai IN
09 1KORES (INDIA) LIMITED Navi Mumbai IN
10 2MYLAN LABORATORIES LIMITED Hyderabad IN
11 1QUIMICA SINTETICA S.A. Alcala De Henares ES
12 1SREEPATHI PHARMACEUTICALS LIMITED Hyderabad IN
13 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
14 1Smruthi Organics Limited Solapur IN
15 1Uquifa Mexico S.A. de C.V. Jiutepec MX
16 2ZHEJIANG GUOBANG PHARMACEUTICAL CO., LTD. Shaoxing CN
17 1ZHEJIANG JINGXIN PHARMACEUTICAL CO., LTD. Xinchang CN
Neuland Laboratories- A dedicated 100% API provider.
Certificate Number : CEP 2000-405 - Rev 13
Status : Valid
Issue Date : 2024-10-16
Type : Chemical
Substance Number : 888
65
PharmaCompass offers a list of Ciprofloxacin 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 Ciprofloxacin Hydrochloride manufacturer or Ciprofloxacin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ciprofloxacin Hydrochloride manufacturer or Ciprofloxacin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Ciprofloxacin Hydrochloride API Price utilized in the formulation of products. Ciprofloxacin Hydrochloride API Price is not always fixed or binding as the Ciprofloxacin Hydrochloride Price is obtained through a variety of data sources. The Ciprofloxacin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cipro manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cipro, including repackagers and relabelers. The FDA regulates Cipro manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cipro 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 Cipro manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cipro supplier is an individual or a company that provides Cipro active pharmaceutical ingredient (API) or Cipro finished formulations upon request. The Cipro suppliers may include Cipro API manufacturers, exporters, distributors and traders.
click here to find a list of Cipro suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cipro CEP of the European Pharmacopoeia monograph is often referred to as a Cipro Certificate of Suitability (COS). The purpose of a Cipro CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cipro EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cipro to their clients by showing that a Cipro CEP has been issued for it. The manufacturer submits a Cipro CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cipro CEP holder for the record. Additionally, the data presented in the Cipro CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cipro DMF.
A Cipro CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cipro 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 Cipro suppliers with CEP (COS) on PharmaCompass.
We have 16 companies offering Cipro
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