Neuland Laboratories- A dedicated 100% API provider.
Reset all filters
01 1Neuland Laboratories
02 2TAPI Technology & API Services
03 2Aurobindo Pharma Limited
04 2Changzhou Pharmaceutical Factory
05 3Glenmark Life Sciences
06 2Hetero Drugs
07 3Lupin Ltd
08 3MSN Laboratories
09 1Macleods Pharmaceuticals Limited
10 1Micro Labs Limited
11 1Raks Pharma
12 1Saptagir Laboratories
13 1Signa S.A. de C.V.
14 1Symed Labs
15 1Viatris
16 1WUHAN ZY PHARMACEUTICAL CO LTD
17 1Waterstone Pharmaceuticals Inc.
18 1Zhejiang Jingsheng Pharmaceutical
19 1Zhejiang Tianyu Pharmaceutical Co., Ltd
Reset all filters
01 9EZETIMIBE
02 1EZETIMIBE (D067 PROCESS)
03 1EZETIMIBE (FORM-B)
04 1EZETIMIBE (PROCESS I)
05 1EZETIMIBE (ROUTE CODE: ZT)
06 1EZETIMIBE DRUG SUBSTANCE
07 7EZETIMIBE USP
08 1EZETIMIBE USP (FORM-X)
09 1EZETIMIBE USP (PROCESS-B)
10 1EZETIMIBE USP (PROCESS-C)
11 1EZETIMIBE USP (PROCESS-II)
12 1EZETIMIBE USP [ROUTE CODE "EE"]
13 1EZETIMIBE USP [ROUTE CODE - EB]
14 1EZETIMIBE USP [ROUTE CODE - EZ]
15 1EZETIMIBE, USP (PROCESS II)
Reset all filters
01 6China
02 19India
03 2Israel
04 1Mexico
05 1U.S.A
Reset all filters
01 26Active
02 3Inactive
Reset all filters
01 20Complete
02 9Blank
GDUFA
DMF Review : Complete
Rev. Date : 2018-08-14
Pay. Date : 2018-07-05
DMF Number : 25543
Submission : 2011-11-30
Status : Active
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 : 2013-04-17
Pay. Date : 2013-04-04
DMF Number : 20039
Submission : 2006-12-13
Status : Active
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 : 2013-08-06
Pay. Date : 2012-11-08
DMF Number : 26068
Submission : 2012-05-17
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-04-03
Pay. Date : 2013-09-27
DMF Number : 24511
Submission : 2010-12-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19717
Submission : 2006-08-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-03-21
Pay. Date : 2013-11-29
DMF Number : 27303
Submission : 2013-09-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24825
Submission : 2011-04-12
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-06-14
Pay. Date : 2016-05-10
DMF Number : 26972
Submission : 2013-04-01
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-08-13
Pay. Date : 2013-08-01
DMF Number : 21554
Submission : 2008-04-17
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-05-01
Pay. Date : 2013-09-20
DMF Number : 25653
Submission : 2011-12-30
Status : Active
Type : II
15
PharmaCompass offers a list of Ezetimibe 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 Ezetimibe manufacturer or Ezetimibe supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ezetimibe manufacturer or Ezetimibe supplier.
PharmaCompass also assists you with knowing the Ezetimibe API Price utilized in the formulation of products. Ezetimibe API Price is not always fixed or binding as the Ezetimibe Price is obtained through a variety of data sources. The Ezetimibe Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A VYTORIN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of VYTORIN, including repackagers and relabelers. The FDA regulates VYTORIN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. VYTORIN 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 VYTORIN manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A VYTORIN supplier is an individual or a company that provides VYTORIN active pharmaceutical ingredient (API) or VYTORIN finished formulations upon request. The VYTORIN suppliers may include VYTORIN API manufacturers, exporters, distributors and traders.
click here to find a list of VYTORIN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A VYTORIN DMF (Drug Master File) is a document detailing the whole manufacturing process of VYTORIN active pharmaceutical ingredient (API) in detail. Different forms of VYTORIN DMFs exist exist since differing nations have different regulations, such as VYTORIN USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A VYTORIN DMF submitted to regulatory agencies in the US is known as a USDMF. VYTORIN USDMF includes data on VYTORIN's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The VYTORIN USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of VYTORIN suppliers with USDMF on PharmaCompass.
We have 19 companies offering VYTORIN
Get in contact with the supplier of your choice: