SNJ Labs: WHO-GMP certified API leader in India, specializing in bulk drugs & intermediates with unmatched expertise.
01 2SNJ Labs
02 3Biophore India Pharmaceuticals Pvt Ltd
03 1Dr. Reddy's Laboratories
04 2Lupin Manufacturing Solutions
05 1Actavis Inc
06 1Alivus Life Sciences
07 2Apothecon Pharmaceuticals
08 1Biofer
09 1CSL Vifor
10 1Chongqing Pharmaceutical Research Institute Co Ltd
11 1Cilag AG
12 1Emcure Pharmaceuticals
13 1GLAND PHARMA LIMITED
14 1Global Calcium
15 1Hetero Drugs
16 1Nanjing Lifenergy R&D Co Ltd
17 1Opocrin SpA
18 1Shanghai Neutan Pharmaceutical
19 1Sichuan Gowell Pharmaceutical
20 1Sichuan Huiyu Pharmaceutical
21 1Solara Active Pharma Sciences
22 1Suven Pharmaceuticals
23 2Symed Labs
24 2Viatris
25 1Yabao Pharmaceutical Group Co. Ltd
SNJ Labs: WHO-GMP certified API leader in India, specializing in bulk drugs & intermediates with unmatched expertise.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30380
Submission : 2016-01-03
Status :
Type : II
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33643
Submission : 2019-03-30
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2016-08-04
Pay. Date : 2016-07-14
DMF Number : 28865
Submission : 2016-07-07
Status :
Type : II
Lupin Manufacturing Solutions – delivering high-quality APIs & end-to-end CDMO services for faster, cost-effective drug development.
GDUFA
DMF Review : Complete
Rev. Date : 2016-09-20
Pay. Date : 2016-07-05
DMF Number : 30348
Submission : 2016-04-15
Status :
Type : II
SNJ Labs: WHO-GMP certified API leader in India, specializing in bulk drugs & intermediates with unmatched expertise.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34357
Submission : 2019-12-10
Status :
Type : II
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34957
Submission : 2020-06-30
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 : 2023-11-10
Pay. Date : 2023-09-28
DMF Number : 38610
Submission : 2023-07-31
Status :
Type : II
Lupin Manufacturing Solutions – delivering high-quality APIs & end-to-end CDMO services for faster, cost-effective drug development.
GDUFA
DMF Review : Complete
Rev. Date : 2024-11-19
Pay. Date : 2024-10-30
DMF Number : 39674
Submission : 2024-04-06
Status :
Type : II
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PharmaCompass offers a list of Iron Sucrose 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 Iron Sucrose manufacturer or Iron Sucrose supplier for your needs.
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PharmaCompass also assists you with knowing the Iron Sucrose API Price utilized in the formulation of products. Iron Sucrose API Price is not always fixed or binding as the Iron Sucrose Price is obtained through a variety of data sources. The Iron Sucrose Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Encifer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Encifer, including repackagers and relabelers. The FDA regulates Encifer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Encifer 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 Encifer supplier is an individual or a company that provides Encifer active pharmaceutical ingredient (API) or Encifer finished formulations upon request. The Encifer suppliers may include Encifer API manufacturers, exporters, distributors and traders.
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A Encifer DMF (Drug Master File) is a document detailing the whole manufacturing process of Encifer active pharmaceutical ingredient (API) in detail. Different forms of Encifer DMFs exist exist since differing nations have different regulations, such as Encifer USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Encifer DMF submitted to regulatory agencies in the US is known as a USDMF. Encifer USDMF includes data on Encifer's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Encifer USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Encifer suppliers with USDMF on PharmaCompass.
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