Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 2Granules India Limited
02 1Dr. Reddy's Laboratories
03 1Moehs Iberica
04 1TAPI Technology & API Services
05 1Aarti Drugs
06 1Actavis Inc
07 1Alembic Pharmaceuticals Limited
08 1Arevipharma
09 1AstraZeneca
10 1Aurobindo Pharma Limited
11 1CTX Lifesciences
12 1Esteve Quimica
13 1HEC Pharm
14 1Hetero Drugs
15 1Indoco Remedies Limited
16 2Ipca Laboratories
17 1Kopran
18 1MSN Laboratories
19 1Macleods Pharmaceuticals Limited
20 1Polydrug Laboratories Private Limited
21 2Sun Pharmaceutical Industries Limited
22 1Syn-Tech Chem. & Pharm
23 1Unichem Laboratories Limited
24 2YUNG ZIP CHEMICAL INDUSTRIAL
25 1Zentiva
26 1Zhejiang Apeloa Jiayuan Pharmaceutical
27 1Zhejiang Hisoar Pharmaceutical
28 1Zhejiang Huahai Pharmaceutical
29 1Zhejiang Yongtai Technology
30 1Zydus Lifesciences
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
GDUFA
DMF Review : Complete
Rev. Date : 2021-05-27
Pay. Date : 2021-04-19
DMF Number : 33544
Submission : 2019-03-27
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2024-03-19
Pay. Date : 2024-02-28
DMF Number : 18348
Submission : 2005-05-13
Status :
Type : II
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-12
Pay. Date : 2013-09-23
DMF Number : 16621
Submission : 2003-06-19
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 : 2013-09-04
Pay. Date : 2013-06-19
DMF Number : 14612
Submission : 1999-12-09
Status :
Type : II
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35959
Submission : 2021-06-13
Status :
Type : II
80
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A Seloken ZOC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Seloken ZOC, including repackagers and relabelers. The FDA regulates Seloken ZOC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Seloken ZOC 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 Seloken ZOC supplier is an individual or a company that provides Seloken ZOC active pharmaceutical ingredient (API) or Seloken ZOC finished formulations upon request. The Seloken ZOC suppliers may include Seloken ZOC API manufacturers, exporters, distributors and traders.
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A Seloken ZOC DMF (Drug Master File) is a document detailing the whole manufacturing process of Seloken ZOC active pharmaceutical ingredient (API) in detail. Different forms of Seloken ZOC DMFs exist exist since differing nations have different regulations, such as Seloken ZOC USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Seloken ZOC DMF submitted to regulatory agencies in the US is known as a USDMF. Seloken ZOC USDMF includes data on Seloken ZOC's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Seloken ZOC USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 30 companies offering Seloken ZOC
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