DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
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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 1SMS LIFESCIENCES INDIA LIMITED Hyderabad IN
15 2SMS PHARMACEUTICALS LIMITED Hyderabad IN
16 1SULESHVARI PHARMA Ankleshwar IN
17 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
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01 15Famotidine
02 1Famotidine, FM3 Process
03 1Famotidine, Form B
04 1Famotidine, Unit-VII
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01 1Hungary
02 15India
03 1Spain
04 1Blank
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01 16Valid
02 2Withdrawn 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 : R1-CEP 2009-161 - Rev 01
Status : Valid
Issue Date : 2023-05-31
Type : Chemical
Substance Number : 1012
Certificate Number : CEP 2015-216 - Rev 01
Status : Valid
Issue Date : 2025-05-16
Type : Chemical
Substance Number : 1012
Certificate Number : CEP 2023-307 - Rev 00
Status : Valid
Issue Date : 2025-02-26
Type : Chemical
Substance Number : 1012
Certificate Number : CEP 2021-367 - Rev 01
Status : Valid
Issue Date : 2024-10-02
Type : Chemical
Substance Number : 1012
Certificate Number : CEP 2022-213 - Rev 01
Status : Valid
Issue Date : 2023-10-19
Type : Chemical
Substance Number : 1012
Certificate Number : R0-CEP 2021-134 - Rev 00
Status : Valid
Issue Date : 2023-01-03
Type : Chemical
Substance Number : 1012
Certificate Number : CEP 2017-307 - Rev 03
Status : Valid
Issue Date : 2024-05-13
Type : Chemical
Substance Number : 1012
Certificate Number : R0-CEP 2022-307 - Rev 00
Status : Valid
Issue Date : 2023-08-30
Type : Chemical
Substance Number : 1012
Certificate Number : R0-CEP 2021-503 - Rev 00
Status : Valid
Issue Date : 2023-07-03
Type : Chemical
Substance Number : 1012
Certificate Number : R1-CEP 2009-080 - Rev 03
Status : Valid
Issue Date : 2019-09-16
Type : Chemical
Substance Number : 1012
94
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 AC-11713 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AC-11713, including repackagers and relabelers. The FDA regulates AC-11713 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AC-11713 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 AC-11713 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AC-11713 supplier is an individual or a company that provides AC-11713 active pharmaceutical ingredient (API) or AC-11713 finished formulations upon request. The AC-11713 suppliers may include AC-11713 API manufacturers, exporters, distributors and traders.
click here to find a list of AC-11713 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AC-11713 CEP of the European Pharmacopoeia monograph is often referred to as a AC-11713 Certificate of Suitability (COS). The purpose of a AC-11713 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AC-11713 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AC-11713 to their clients by showing that a AC-11713 CEP has been issued for it. The manufacturer submits a AC-11713 CEP (COS) as part of the market authorization procedure, and it takes on the role of a AC-11713 CEP holder for the record. Additionally, the data presented in the AC-11713 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AC-11713 DMF.
A AC-11713 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AC-11713 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 AC-11713 suppliers with CEP (COS) on PharmaCompass.
We have 15 companies offering AC-11713
Get in contact with the supplier of your choice: