DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories
02 1Biophore India Pharmaceuticals Pvt Ltd
03 1TAPI Technology & API Services
04 1Allite (Shanghai) Pharmaceutical Technology
05 1Chongqing Carelife Pharmaceutical
06 1Chongqing Pharmaceutical Research Institute Co Ltd
07 1Chongqing Sintaho Pharmaceutical
08 1Fresenius Kabi Oncology Limited
09 1Hansoh Pharma
10 1Hetero Drugs
11 1Intas Pharmaceuticals
12 1Laurus Labs
13 1Lianyungang Runzhong Pharmaceutical Co Ltd
14 1Lunan Pharmaceutical
15 1MSN Laboratories
16 1Polymed Therapeutics Inc.
17 1Qilu Pharmaceutical
18 1SEACROSS PHARMACEUTICALS
19 1Sichuan Huiyu Pharmaceutical
20 1TONGSHENG
21 1Wisdom Pharmaceutical
22 1Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2016-07-06
Pay. Date : 2016-05-04
DMF Number : 30402
Submission : 2016-03-29
Status :
Type : II
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Complete
Rev. Date : 2024-09-19
Pay. Date : 2024-08-27
DMF Number : 32406
Submission : 2017-12-30
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 : 2016-02-25
Pay. Date : 2015-12-21
DMF Number : 30124
Submission : 2016-01-21
Status :
Type : II
57
PharmaCompass offers a list of Carfilzomib 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 Carfilzomib manufacturer or Carfilzomib supplier for your needs.
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A CAS-868540-17-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-868540-17-4, including repackagers and relabelers. The FDA regulates CAS-868540-17-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-868540-17-4 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 CAS-868540-17-4 supplier is an individual or a company that provides CAS-868540-17-4 active pharmaceutical ingredient (API) or CAS-868540-17-4 finished formulations upon request. The CAS-868540-17-4 suppliers may include CAS-868540-17-4 API manufacturers, exporters, distributors and traders.
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A CAS-868540-17-4 DMF (Drug Master File) is a document detailing the whole manufacturing process of CAS-868540-17-4 active pharmaceutical ingredient (API) in detail. Different forms of CAS-868540-17-4 DMFs exist exist since differing nations have different regulations, such as CAS-868540-17-4 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A CAS-868540-17-4 DMF submitted to regulatory agencies in the US is known as a USDMF. CAS-868540-17-4 USDMF includes data on CAS-868540-17-4's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CAS-868540-17-4 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 21 companies offering CAS-868540-17-4
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