DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories
02 1ALP Pharm
03 1Aurisco Pharmaceutical
04 1Aurobindo Pharma Limited
05 1Cdymax
06 1Chongqing Pharmaceutical Research Institute Co Ltd
07 2Cipla
08 1Hetero Drugs
09 1Hubei Biocause Heilen Pharmaceutical Co., Ltd
10 1Hubei Gedian Humanwell Pharmaceutical
11 2Industriale Chimica
12 3MSN Laboratories
13 1Olon S.p.A
14 1Qilu Antibiotics Pharmaceutical Co., Ltd.
15 1Raks Pharma
16 1ScinoPharm Taiwan Ltd
17 1Shandong Sito Bio-technology Co ltd
18 2Sterling Spa
19 1Sun Pharmaceutical Industries Limited
20 1Teva Pharmaceutical Industries
21 1Tianjin Weijie Pharmaceutical Co., Ltd.
22 1Zhejiang Shenzhou Pharmaceutical
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2014-08-13
Pay. Date : 2014-05-05
DMF Number : 28038
Submission : 2014-03-27
Status :
Type : II
23
PharmaCompass offers a list of Abiraterone Acetate 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 Abiraterone Acetate manufacturer or Abiraterone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Abiraterone Acetate manufacturer or Abiraterone Acetate supplier.
PharmaCompass also assists you with knowing the Abiraterone Acetate API Price utilized in the formulation of products. Abiraterone Acetate API Price is not always fixed or binding as the Abiraterone Acetate Price is obtained through a variety of data sources. The Abiraterone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zytiga manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zytiga, including repackagers and relabelers. The FDA regulates Zytiga manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zytiga 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 Zytiga manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zytiga supplier is an individual or a company that provides Zytiga active pharmaceutical ingredient (API) or Zytiga finished formulations upon request. The Zytiga suppliers may include Zytiga API manufacturers, exporters, distributors and traders.
click here to find a list of Zytiga suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zytiga DMF (Drug Master File) is a document detailing the whole manufacturing process of Zytiga active pharmaceutical ingredient (API) in detail. Different forms of Zytiga DMFs exist exist since differing nations have different regulations, such as Zytiga USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Zytiga DMF submitted to regulatory agencies in the US is known as a USDMF. Zytiga USDMF includes data on Zytiga's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Zytiga USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Zytiga suppliers with USDMF on PharmaCompass.
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