Neuland Laboratories- A dedicated 100% API provider.
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
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)
01 6China
02 19India
03 2Israel
04 1Mexico
05 1U.S.A
01 26Active
02 3Inactive
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 : 24825
Submission : 2011-04-12
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 : 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
A Zetia manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zetia, including repackagers and relabelers. The FDA regulates Zetia manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zetia 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 Zetia manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zetia supplier is an individual or a company that provides Zetia active pharmaceutical ingredient (API) or Zetia finished formulations upon request. The Zetia suppliers may include Zetia API manufacturers, exporters, distributors and traders.
click here to find a list of Zetia suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zetia DMF (Drug Master File) is a document detailing the whole manufacturing process of Zetia active pharmaceutical ingredient (API) in detail. Different forms of Zetia DMFs exist exist since differing nations have different regulations, such as Zetia USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Zetia DMF submitted to regulatory agencies in the US is known as a USDMF. Zetia USDMF includes data on Zetia's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Zetia USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Zetia suppliers with USDMF on PharmaCompass.
We have 19 companies offering Zetia
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