01 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1ARCH PHARMALABS LIMITED Mumbai IN
03 1ARENE LIFE SCIENCES PRIVATE LIMITED Sangareddy IN
04 1CIPLA LIMITED Mumbai IN
05 3HETERO LABS LIMITED Hyderabad IN
06 2LAURUS LABS LIMITED Hyderabad IN
07 1MYLAN LABORATORIES LIMITED Hyderabad IN
08 2SHANGHAI DESANO CHEMICAL PHARMACEUTICAL CO., LTD. Laogang Town CN
09 1SHIJIAZHUANG LONZEAL PHARMACEUTICALS CO., LTD. Shenze CN
10 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
11 1VIVIN DRUGS & PHARMACEUTICALS PRIVATE LIMITED Hyderabad IN
01 9Lamivudine
02 1Lamivudine, Form II
03 1Lamivudine, Form-II, Process-II
04 1Lamivudine, LAN process, Form II
05 1Lamivudine, LML Process
06 1Lamivudine, Process 1
07 1Lamivudine, Process C
08 1Lamivudine, SVL Process
01 3China
02 12India
03 1U.S.A
01 15Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2012-362 - Rev 00
Status : Valid
Issue Date : 2021-09-14
Type : Chemical
Substance Number : 2217
Certificate Number : CEP 2022-248 - Rev 01
Status : Valid
Issue Date : 2024-09-18
Type : Chemical
Substance Number : 2217
Certificate Number : R1-CEP 2007-103 - Rev 03
Status : Valid
Issue Date : 2018-01-05
Type : Chemical
Substance Number : 2217
Certificate Number : R1-CEP 2008-160 - Rev 02
Status : Valid
Issue Date : 2017-08-10
Type : Chemical
Substance Number : 2217
Lamivudine, LAN Process, Form II
Certificate Number : CEP 2013-168 - Rev 01
Status : Valid
Issue Date : 2024-05-02
Type : Chemical
Substance Number : 2217
Certificate Number : R0-CEP 2019-082 - Rev 01
Status : Valid
Issue Date : 2023-03-20
Type : Chemical
Substance Number : 2217
Certificate Number : R1-CEP 2016-045 - Rev 01
Status : Valid
Issue Date : 2023-01-24
Type : Chemical
Substance Number : 2217
Certificate Number : CEP 2019-133 - Rev 03
Status : Valid
Issue Date : 2025-02-26
Type : Chemical
Substance Number : 2217
Certificate Number : R0-CEP 2023-119 - Rev 00
Status : Valid
Issue Date : 2023-06-30
Type : Chemical
Substance Number : 2217
Certificate Number : R0-CEP 2019-001 - Rev 00
Status : Valid
Issue Date : 2021-04-01
Type : Chemical
Substance Number : 2217
78
PharmaCompass offers a list of Lamivudine 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 Lamivudine manufacturer or Lamivudine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lamivudine manufacturer or Lamivudine supplier.
PharmaCompass also assists you with knowing the Lamivudine API Price utilized in the formulation of products. Lamivudine API Price is not always fixed or binding as the Lamivudine Price is obtained through a variety of data sources. The Lamivudine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Heptovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Heptovir, including repackagers and relabelers. The FDA regulates Heptovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Heptovir 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 Heptovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Heptovir supplier is an individual or a company that provides Heptovir active pharmaceutical ingredient (API) or Heptovir finished formulations upon request. The Heptovir suppliers may include Heptovir API manufacturers, exporters, distributors and traders.
click here to find a list of Heptovir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Heptovir CEP of the European Pharmacopoeia monograph is often referred to as a Heptovir Certificate of Suitability (COS). The purpose of a Heptovir CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Heptovir EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Heptovir to their clients by showing that a Heptovir CEP has been issued for it. The manufacturer submits a Heptovir CEP (COS) as part of the market authorization procedure, and it takes on the role of a Heptovir CEP holder for the record. Additionally, the data presented in the Heptovir CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Heptovir DMF.
A Heptovir CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Heptovir 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 Heptovir suppliers with CEP (COS) on PharmaCompass.
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