DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 1NEULAND LABORATORIES LIMITED Hyderabad IN
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1HETERO DRUGS LIMITED Hyderabad IN
05 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
06 1MSN LIFE SCIENCES PRIVATE LIMITED Chandampet Village IN
07 2QUIMICA SINTETICA S.A. Alcala De Henares ES
08 1SAURAV CHEMICALS LIMITED Bhagwanpura Village IN
09 1SHAOXING JINGXIN PHARMACEUTICAL CO., LTD. Shangyu CN
10 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
11 1ZHEJIANG APELOA KANGYU PHARMACEUTICAL CO., LTD. Hengdian CN
12 1ZHEJIANG LANGHUA PHARMACEUTICAL CO., LTD. Linhai CN
13 1ZHEJIANG STARRY PHARMACEUTICAL CO., LTD. Xianju CN
14 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
15 1Zhejiang East-Asia Pharmaceutical Co., Ltd. Taizhou CN
01 14Levofloxacin hemihydrate
02 1Levofloxacin hemihydrate, Monoclinic form
03 1Levofloxacin hemihydrate, Process II
01 5China
02 9India
03 2Spain
01 15Valid
02 1Withdrawn by Holder
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R0-CEP 2019-059 - Rev 01
Status : Valid
Issue Date : 2021-12-21
Type : Chemical
Substance Number : 2598
Certificate Number : CEP 2019-023 - Rev 04
Status : Valid
Issue Date : 2023-11-07
Type : Chemical
Substance Number : 2598
Levofloxacin Hemihydrate, Process II
Certificate Number : CEP 2021-284 - Rev 01
Status : Valid
Issue Date : 2023-11-23
Type : Chemical
Substance Number : 2598
Certificate Number : R0-CEP 2019-315 - Rev 00
Status : Valid
Issue Date : 2022-05-18
Type : Chemical
Substance Number : 2598
Certificate Number : CEP 2019-161 - Rev 03
Status : Valid
Issue Date : 2024-07-17
Type : Chemical
Substance Number : 2598
Certificate Number : R0-CEP 2020-128 - Rev 00
Status : Valid
Issue Date : 2021-07-16
Type : Chemical
Substance Number : 2598
Certificate Number : R0-CEP 2020-242 - Rev 01
Status : Valid
Issue Date : 2023-06-22
Type : Chemical
Substance Number : 2598
Certificate Number : CEP 2020-041 - Rev 02
Status : Valid
Issue Date : 2024-01-26
Type : Chemical
Substance Number : 2598
Certificate Number : CEP 2019-111 - Rev 02
Status : Valid
Issue Date : 2023-11-29
Type : Chemical
Substance Number : 2598
Certificate Number : R0-CEP 2022-059 - Rev 00
Status : Valid
Issue Date : 2023-08-30
Type : Chemical
Substance Number : 2598
A Levofloxacin Hemihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levofloxacin Hemihydrate, including repackagers and relabelers. The FDA regulates Levofloxacin Hemihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levofloxacin Hemihydrate 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 Levofloxacin Hemihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levofloxacin Hemihydrate supplier is an individual or a company that provides Levofloxacin Hemihydrate active pharmaceutical ingredient (API) or Levofloxacin Hemihydrate finished formulations upon request. The Levofloxacin Hemihydrate suppliers may include Levofloxacin Hemihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Levofloxacin Hemihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levofloxacin Hemihydrate CEP of the European Pharmacopoeia monograph is often referred to as a Levofloxacin Hemihydrate Certificate of Suitability (COS). The purpose of a Levofloxacin Hemihydrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Levofloxacin Hemihydrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Levofloxacin Hemihydrate to their clients by showing that a Levofloxacin Hemihydrate CEP has been issued for it. The manufacturer submits a Levofloxacin Hemihydrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Levofloxacin Hemihydrate CEP holder for the record. Additionally, the data presented in the Levofloxacin Hemihydrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Levofloxacin Hemihydrate DMF.
A Levofloxacin Hemihydrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Levofloxacin Hemihydrate 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 Levofloxacin Hemihydrate suppliers with CEP (COS) on PharmaCompass.
We have 15 companies offering Levofloxacin Hemihydrate
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