Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1FARMAK, a.s
02 1Seqens
03 1Cohance Lifesciences
04 1Neuland Laboratories
05 1Kinsy SL
06 1Actavis Inc
07 1Anhui Sinotech Industrial
08 1Arevipharma
09 1Beiersdorf AG
10 1Boehringer Ingelheim GmbH
11 1Jin Dun Medical
12 1Micro Labs Limited
13 1Nantong Jinghua Pharmaceutical
14 1Xian Wanlong Pharmaceutical Co. Ltd
01 4China
02 1Czech Republic
03 1France
04 3Germany
05 3India
06 1Ireland
07 1Spain
01 2Inactive
02 12Blank
01 1Expired
02 5Valid
03 1Withdrawn by Holder
04 7Blank
01 14Blank
01 1WC-0037
02 1WC-0225A3
03 12Blank
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Certificate Number : CEP 2008-266 - Rev 03
Issue Date : 2023-09-22
Type : Chemical
Substance Number : 1758
Status : Valid
Available Reg Filing : ASMF |
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Certificate Number : CEP 2005-009 - Rev 11
Issue Date : 2024-10-23
Type : Chemical
Substance Number : 1758
Status : Valid
Available Reg Filing : ASMF |
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : CEP 2013-175 - Rev 03
Issue Date : 2024-01-30
Type : Chemical
Substance Number : 1758
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-06-16
Written Confirmation Number : WC-0037
Address of the Firm :
Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
Certificate Number : R1-CEP 2014-357 - Rev 00
Issue Date : 2021-06-10
Type : Chemical
Substance Number : 1758
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12863
Submission : 1998-02-13
Status : Inactive
Type : II
Certificate Number : R1-CEP 2003-139 - Rev 00
Issue Date : 2009-07-29
Type : Chemical
Substance Number : 1758
Status : Withdrawn by Holder
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7702
Submission : 1988-10-11
Status : Inactive
Type : II
Certificate Number : R0-CEP 2005-292 - Rev 00
Issue Date : 2007-06-01
Type : Chemical
Substance Number : 1758
Status : Expired
Certificate Number : R1-CEP 2013-122 - Rev 00
Issue Date : 2020-01-09
Type : Chemical
Substance Number : 1758
Status : Valid
Date of Issue : 2020-01-16
Valid Till : 2022-08-15
Written Confirmation Number : WC-0225A3
Address of the Firm :
A Moxonidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Moxonidine, including repackagers and relabelers. The FDA regulates Moxonidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Moxonidine 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 Moxonidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Moxonidine supplier is an individual or a company that provides Moxonidine active pharmaceutical ingredient (API) or Moxonidine finished formulations upon request. The Moxonidine suppliers may include Moxonidine API manufacturers, exporters, distributors and traders.
click here to find a list of Moxonidine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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