01 1Alembic Pharmaceuticals Limited
02 1Cipla
03 1Emcure Pharmaceuticals
04 1Formosa Laboratories
05 1Maprimed
06 1Unichem Laboratories Limited
01 3LEFLUNOMIDE
02 3LEFLUNOMIDE USP
01 1Argentina
02 4India
03 1Taiwan
01 5Active
02 1Inactive
01 3Complete
02 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16112
Submission : 2002-08-29
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-02-18
Pay. Date : 2015-08-21
DMF Number : 16109
Submission : 2002-08-23
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16124
Submission : 2002-09-06
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-03-07
Pay. Date : 2016-08-04
DMF Number : 16038
Submission : 2002-06-27
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-12-16
Pay. Date : 2018-09-04
DMF Number : 32988
Submission : 2018-09-07
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16504
Submission : 2003-03-25
Status : Inactive
Type : II
45
PharmaCompass offers a list of Leflunomide 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 Leflunomide manufacturer or Leflunomide supplier for your needs.
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PharmaCompass also assists you with knowing the Leflunomide API Price utilized in the formulation of products. Leflunomide API Price is not always fixed or binding as the Leflunomide Price is obtained through a variety of data sources. The Leflunomide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EU-0100649 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EU-0100649, including repackagers and relabelers. The FDA regulates EU-0100649 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EU-0100649 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 EU-0100649 supplier is an individual or a company that provides EU-0100649 active pharmaceutical ingredient (API) or EU-0100649 finished formulations upon request. The EU-0100649 suppliers may include EU-0100649 API manufacturers, exporters, distributors and traders.
click here to find a list of EU-0100649 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A EU-0100649 DMF (Drug Master File) is a document detailing the whole manufacturing process of EU-0100649 active pharmaceutical ingredient (API) in detail. Different forms of EU-0100649 DMFs exist exist since differing nations have different regulations, such as EU-0100649 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A EU-0100649 DMF submitted to regulatory agencies in the US is known as a USDMF. EU-0100649 USDMF includes data on EU-0100649's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The EU-0100649 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of EU-0100649 suppliers with USDMF on PharmaCompass.
We have 6 companies offering EU-0100649
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