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
01 1Ciprofloxacin
02 18Ciprofloxacin Hydrochloride
03 1Ciprofloxacin Hydrochloride, Process 105
01 4China
02 1Gabon
03 1Germany
04 11India
05 1Spain
06 2U.S.A
01 1Expired
02 9Valid
03 1Withdrawn by EDQM Failure to CEP procedure
04 9Withdrawn by Holder
Certificate Number : CEP 2000-405 - Rev 13
Status : Valid
Issue Date : 2024-10-16
Type : Chemical
Substance Number : 888
Certificate Number : CEP 2005-119 - Rev 06
Status : Valid
Issue Date : 2025-01-15
Type : Chemical
Substance Number : 888
Certificate Number : CEP 1998-103 - Rev 07
Status : Valid
Issue Date : 2025-01-22
Type : Chemical
Substance Number : 888
Certificate Number : R1-CEP 2005-045 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2012-09-19
Type : Chemical
Substance Number : 888
Certificate Number : CEP 1999-096 - Rev 09
Status : Valid
Issue Date : 2024-10-30
Type : Chemical
Substance Number : 888
Certificate Number : CEP 1998-090 - Rev 13
Status : Valid
Issue Date : 2024-10-15
Type : Chemical
Substance Number : 888
Certificate Number : CEP 2004-174 - Rev 05
Status : Valid
Issue Date : 2024-03-20
Type : Chemical
Substance Number : 888
Certificate Number : CEP 2003-013 - Rev 08
Status : Valid
Issue Date : 2024-12-11
Type : Chemical
Substance Number : 888
Ciprofloxacin Hydrochloride, Process 105
Certificate Number : CEP 2019-007 - Rev 04
Status : Valid
Issue Date : 2024-10-29
Type : Chemical
Substance Number : 888
Certificate Number : CEP 2010-099 - Rev 04
Status : Valid
Issue Date : 2024-10-30
Type : Chemical
Substance Number : 888
A Ciprofloxacin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ciprofloxacin Hydrochloride, including repackagers and relabelers. The FDA regulates Ciprofloxacin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ciprofloxacin Hydrochloride 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 Ciprofloxacin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ciprofloxacin Hydrochloride supplier is an individual or a company that provides Ciprofloxacin Hydrochloride active pharmaceutical ingredient (API) or Ciprofloxacin Hydrochloride finished formulations upon request. The Ciprofloxacin Hydrochloride suppliers may include Ciprofloxacin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ciprofloxacin Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ciprofloxacin Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Ciprofloxacin Hydrochloride Certificate of Suitability (COS). The purpose of a Ciprofloxacin Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ciprofloxacin Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ciprofloxacin Hydrochloride to their clients by showing that a Ciprofloxacin Hydrochloride CEP has been issued for it. The manufacturer submits a Ciprofloxacin Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ciprofloxacin Hydrochloride CEP holder for the record. Additionally, the data presented in the Ciprofloxacin Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ciprofloxacin Hydrochloride DMF.
A Ciprofloxacin Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ciprofloxacin Hydrochloride 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 Ciprofloxacin Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 16 companies offering Ciprofloxacin Hydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?