European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
01 1Polpharma
02 1Dr. Reddy's Laboratories
03 1Minakem (formerly Delmar Chemicals)
04 1Metrochem API Private Limited
05 1Aarti Pharmalabs
06 2Neuland Laboratories
07 1TAPI Technology & API Services
08 1Honour Lab Limited
09 1ALP Pharm
10 1Actavis Inc
11 1Alembic Pharmaceuticals Limited
12 1Alivus Life Sciences
13 1Amoli Organics
14 1Apotex Pharmachem
15 1Aurobindo Pharma Limited
16 1Biocon
17 1Changzhou Pharmaceutical Factory
18 1Cipla
19 1Emnar Pharma
20 1HEC Pharm
21 1Hikal
22 1Indoco Remedies Limited
23 1Jiangxi Synergy Pharmaceutical
24 1Jubilant Generics
25 2MSN Laboratories
26 1Macleods Pharmaceuticals Limited
27 1Medichem S.A
28 1Micro Labs Limited
29 3Morepen Laboratories
30 1Natco Pharma
31 1Ningbo Menovo Pharmaceutical
32 1Optimus Pharma
33 1Rakshit Drugs
34 1SINTENOVO, S.A. DE C.V.
35 1SMS Pharmaceuticals
36 2ScinoPharm Taiwan Ltd
37 1Sigmapharm Laboratories, LLC
38 2Srini Pharmaceuticals
39 1Sun Pharmaceutical Industries Limited
40 1Teva Pharmaceutical Industries
41 1Unichem Laboratories Limited
42 1Viatris
43 1Viyash Life Sciences
44 1Zhejiang Guobang Pharmaceutical
45 1Zhejiang Hisun Pharmaceutical
46 1Zhejiang Huahai Pharmaceutical
47 1Zhejiang Jingxin Pharmaceutical
48 1Zhejiang Supor Pharmaceuticals Co., LTD
49 1Zhejiang Tianyu Pharmaceutical Co., Ltd
50 1Zydus Lifesciences
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
GDUFA
DMF Review : Complete
Rev. Date : 2017-02-10
Pay. Date : 2016-12-20
DMF Number : 31166
Submission : 2016-11-16
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2016-03-11
Pay. Date : 2015-09-30
DMF Number : 29707
Submission : 2015-09-22
Status :
Type : II
Minakem is manufacturing small molecules APIs including corticosteroids
GDUFA
DMF Review : Complete
Rev. Date : 2016-08-15
Pay. Date : 2016-03-28
DMF Number : 30336
Submission : 2016-03-14
Status :
Type : II
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35518
Submission : 2020-12-30
Status :
Type : II
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35969
Submission : 2021-07-01
Status :
Type : II
Neuland Laboratories- A dedicated 100% API provider.
GDUFA
DMF Review : Complete
Rev. Date : 2018-07-16
Pay. Date : 2018-06-13
DMF Number : 32422
Submission : 2018-01-31
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 : 41922
Submission : 2025-06-17
Status :
Type : II
Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
GDUFA
DMF Review : Complete
Rev. Date : 2016-07-05
Pay. Date : 2016-04-26
DMF Number : 30461
Submission : 2016-05-18
Status :
Type : II
Neuland Laboratories- A dedicated 100% API provider.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39444
Submission : 2024-01-31
Status :
Type : II
49
PharmaCompass offers a list of Apixaban 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 Apixaban manufacturer or Apixaban supplier for your needs.
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A cc-395 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of cc-395, including repackagers and relabelers. The FDA regulates cc-395 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. cc-395 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 cc-395 supplier is an individual or a company that provides cc-395 active pharmaceutical ingredient (API) or cc-395 finished formulations upon request. The cc-395 suppliers may include cc-395 API manufacturers, exporters, distributors and traders.
click here to find a list of cc-395 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A cc-395 DMF (Drug Master File) is a document detailing the whole manufacturing process of cc-395 active pharmaceutical ingredient (API) in detail. Different forms of cc-395 DMFs exist exist since differing nations have different regulations, such as cc-395 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A cc-395 DMF submitted to regulatory agencies in the US is known as a USDMF. cc-395 USDMF includes data on cc-395's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The cc-395 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of cc-395 suppliers with USDMF on PharmaCompass.
We have 50 companies offering cc-395
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