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Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications. 
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01 Minakem (2)
02 Metrochem API Private Limited (2)
03 Dr. Reddy's Laboratories (3)
04 RANBAXY LABORATORIES LIMITED (1)
05 Sun Pharmaceutical Industries Limited (2)
06 Alkem Laboratories (2)
07 Aurobindo Pharma Limited (2)
08 Chromo Laboratories (1)
09 Cipla (2)
10 Everest Organics (1)
11 F.I.S. Fabbrica Italiana Sintetici (3)
12 Glenmark Life Sciences (4)
13 Granules India Limited (2)
14 HEC Pharm (1)
15 Hetero Drugs (5)
16 Jubilant Generics (5)
17 Lee Pharma (1)
18 Lupin Ltd (1)
19 MSN Laboratories (3)
20 Macleods Pharmaceuticals Limited (2)
21 Ningbo Menovo Pharmaceutical (1)
22 Perrigo API India Private Limited (1)
23 Raks Pharma (2)
24 Shouguang Fukang Pharmaceutical Co., Ltd (2)
25 Srini Pharmaceuticals (1)
26 Torrent Pharmaceuticals Limited (2)
27 UQUIFA (1)
28 Vasudha Pharma Chem (1)
29 Viatris (3)
30 ZHEJIANG JINHUA CONBA BIO-PHARM. CO., LTD. (1)
31 Zhejiang Yongtai Technology (1)
32 Zydus Lifesciences (2)
01 ESOMEPRAZOLE (1)
02 ESOMEPRAZOLE MAGNESIUM (1)
03 ESOMEPRAZOLE MAGNESIUM (AMORPHOUS) USP (1)
04 ESOMEPRAZOLE MAGNESIUM (AMORPHOUS, NON-STERILE BULK DRUG SUBSTANCE) (1)
05 ESOMEPRAZOLE MAGNESIUM AMORPHOUS (PROCESS-2) USP (1)
06 ESOMEPRAZOLE MAGNESIUM AMORPHOUS-USP (1)
07 ESOMEPRAZOLE MAGNESIUM DELAYED - RELEASE PELLETS (1)
08 ESOMEPRAZOLE MAGNESIUM DELAYED-RELEASE PELLETS (25.82% W/W) (1)
09 ESOMEPRAZOLE MAGNESIUM DELAYED-RELEASE PELLETS (AS 20.94%W/W OF ESOMEPRAZOLE) (1)
10 ESOMEPRAZOLE MAGNESIUM DIHYDRATE (13)
11 ESOMEPRAZOLE MAGNESIUM DIHYDRATE (PROCESS II) (2)
12 ESOMEPRAZOLE MAGNESIUM DIHYDRATE (PROCESS-III) (1)
13 ESOMEPRAZOLE MAGNESIUM DIHYDRATE MICRONIZED AND NON MICRONIZED (1)
14 ESOMEPRAZOLE MAGNESIUM DIHYDRATE NON-STERILE BULK DRUG SUBSTANCE (1)
15 ESOMEPRAZOLE MAGNESIUM DIHYDRATE PROCESS II (1)
16 ESOMEPRAZOLE MAGNESIUM DIHYDRATE USP (4)
17 ESOMEPRAZOLE MAGNESIUM TRIHYDRATE (8)
18 ESOMEPRAZOLE MAGNESIUM TRIHYDRATE USP (10)
19 ESOMEPRAZOLE MAGNESIUM TRIHYDRATE, USP (3)
20 ESOMEPRAZOLE MAGNESIUM TRIHYDRATE, USP (ROUTE CODE - "ES") (1)
21 ESOMEPRAZOLE MAGNESIUM USP (2)
22 ESOMEPRAZOLE MAGNESIUM USP (AMORPHOUS) (1)
23 ESOMEPRAZOLE MAGNESIUM USP (AMORPHOUS) (PROCESS I) (1)
24 ESOMEPRAZOLE MAGNESIUM USP (AMORPHOUS) (PROCESS II) (1)
25 ESOMEPRAZOLE MAGNESIUM USP (DIHYDRATE) [ROUTE CODE EP] (1)
26 ESOMEPRAZOLE MAGNESIUM USP (TRIHYDRATE) [ROUTE CODE 'EG'] (1)
27 ESOMEPRAZOLE MAGNESIUM USP, NON-STERILE, BULK DRUG SUBSTANCE (1)
28 ESOMEPRAZOLE POTASSIUM (1)
01 China (6)
02 France (2)
03 India (48)
04 Italy (3)
05 Spain (1)
06 U.S.A (3)
01 Active (55)
02 Inactive (8)
01 Complete (39)
02 Blank (24)
15
PharmaCompass offers a list of Esomeprazole Magnesium 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 Esomeprazole Magnesium manufacturer or Esomeprazole Magnesium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Esomeprazole Magnesium manufacturer or Esomeprazole Magnesium supplier.
PharmaCompass also assists you with knowing the Esomeprazole Magnesium API Price utilized in the formulation of products. Esomeprazole Magnesium API Price is not always fixed or binding as the Esomeprazole Magnesium Price is obtained through a variety of data sources. The Esomeprazole Magnesium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nexium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nexium, including repackagers and relabelers. The FDA regulates Nexium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nexium 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 Nexium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nexium supplier is an individual or a company that provides Nexium active pharmaceutical ingredient (API) or Nexium finished formulations upon request. The Nexium suppliers may include Nexium API manufacturers, exporters, distributors and traders.
click here to find a list of Nexium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nexium DMF (Drug Master File) is a document detailing the whole manufacturing process of Nexium active pharmaceutical ingredient (API) in detail. Different forms of Nexium DMFs exist exist since differing nations have different regulations, such as Nexium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nexium DMF submitted to regulatory agencies in the US is known as a USDMF. Nexium USDMF includes data on Nexium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nexium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Nexium suppliers with USDMF on PharmaCompass.
We have 32 companies offering Nexium
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