Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 1Centrient Pharmaceuticals
02 1Minakem (formerly Delmar Chemicals)
03 3TAPI Technology & API Services
04 1Mankind Pharma
05 2Alivus Life Sciences
06 2Amoli Organics
07 1Apotex Pharmachem
08 2Aurobindo Pharma Limited
09 3Biocon
10 1CTX Lifesciences
11 2Changzhou Pharmaceutical Factory
12 2Chromo Laboratories
13 1HEC Pharm
14 1Hetero Drugs
15 1Innovare Labs
16 1Jubilant Generics
17 1KOLON Life Science, Inc
18 1Lee Pharma
19 3Lek Pharmaceuticals
20 1Lewens Labs
21 1Lupin Ltd
22 4MSN Laboratories
23 1Macleods Pharmaceuticals Limited
24 1Melody Healthcare
25 2Morepen Laboratories
26 1Ningbo Menovo Pharmaceutical
27 1Shanghai Desano Bio-Pharmaceutical
28 1Shanghai Wonder Pharmaceutical
29 1Sun Pharmaceutical Industries Limited
30 1Viatris
31 1ZHEJIANG MENOVO PHARMACEUTICAL CO., LTD. CN 312 369 Shangyu
32 1Zhejiang Hisun Pharmaceutical
33 1Zhejiang Neo-Dankong Pharm. Co.,Ltd.
34 2Zhejiang Yongtai Technology
35 1Zydus Lifesciences
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
GDUFA
DMF Review : Complete
Rev. Date : 2017-11-17
Pay. Date : 2017-05-23
DMF Number : 31410
Submission : 2017-03-28
Status :
Type : II
Minakem is manufacturing small molecules APIs including corticosteroids
GDUFA
DMF Review : Complete
Rev. Date : 2016-04-08
Pay. Date : 2015-09-25
DMF Number : 29190
Submission : 2015-12-03
Status :
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-31
Pay. Date : 2013-01-02
DMF Number : 20671
Submission : 2007-07-12
Status :
Type : II
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
GDUFA
DMF Review : Complete
Rev. Date : 2022-07-11
Pay. Date : 2022-06-07
DMF Number : 36493
Submission : 2021-12-22
Status :
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Complete
Rev. Date : 2016-12-23
Pay. Date : 2016-08-29
DMF Number : 30830
Submission : 2016-12-01
Status :
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27879
Submission : 2014-02-07
Status :
Type : II
11
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A LS-181805 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LS-181805, including repackagers and relabelers. The FDA regulates LS-181805 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LS-181805 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A LS-181805 supplier is an individual or a company that provides LS-181805 active pharmaceutical ingredient (API) or LS-181805 finished formulations upon request. The LS-181805 suppliers may include LS-181805 API manufacturers, exporters, distributors and traders.
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A LS-181805 DMF (Drug Master File) is a document detailing the whole manufacturing process of LS-181805 active pharmaceutical ingredient (API) in detail. Different forms of LS-181805 DMFs exist exist since differing nations have different regulations, such as LS-181805 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A LS-181805 DMF submitted to regulatory agencies in the US is known as a USDMF. LS-181805 USDMF includes data on LS-181805's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The LS-181805 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 35 companies offering LS-181805
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