Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1Moehs Iberica
03 1APEX HEALTHCARE LIMITED
04 1Cambrex Corporation
05 1Delta Synthetic Co. Ltd
06 2Grace
07 1Gufic Biosciences
08 1Harman Finochem
09 1Mahendra Chemicals
10 2Napp Technologies
11 1ORGAMOL PHARMA SOLUTIONS SA
12 2SIMS Srl
13 1Swati Spentose
14 1Syn-Tech Chem. & Pharm
15 1Blank
01 3LIDOCAINE
02 1LIDOCAINE (LIGNOCAINE)
03 1LIDOCAINE BASE
04 1LIDOCAINE BASE / LIDOCAINE HCL
05 1LIDOCAINE BASE CRYSTALLIZED & LIDOCAINE HcL
06 2LIDOCAINE HCL
07 1LIDOCAINE HCL, USP, BP & PH EUR
08 7LIDOCAINE USP
09 1LIDOCAINE, USP
01 1France
02 5India
03 2Italy
04 1Spain
05 1Switzerland
06 2Taiwan
07 5U.S.A
08 1Blank
01 11Active
02 7Inactive
01 7Complete
02 11Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2801
Submission : 1976-11-08
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-03-15
Pay. Date : 2013-02-28
DMF Number : 13235
Submission : 1998-09-25
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19532
Submission : 2006-04-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-04-11
Pay. Date : 2013-03-22
DMF Number : 11339
Submission : 1995-02-10
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-07-11
Pay. Date : 2013-07-05
DMF Number : 11564
Submission : 1995-06-05
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-06-08
Pay. Date : 2013-05-23
DMF Number : 4323
Submission : 1981-11-10
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24050
Submission : 2010-08-09
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4139
Submission : 1981-03-27
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-04-04
Pay. Date : 2014-04-01
DMF Number : 18318
Submission : 2005-04-29
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-10-06
Pay. Date : 2013-09-23
DMF Number : 25830
Submission : 2012-02-22
Status : Active
Type : II
A LIDODERM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LIDODERM, including repackagers and relabelers. The FDA regulates LIDODERM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LIDODERM 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 LIDODERM manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LIDODERM supplier is an individual or a company that provides LIDODERM active pharmaceutical ingredient (API) or LIDODERM finished formulations upon request. The LIDODERM suppliers may include LIDODERM API manufacturers, exporters, distributors and traders.
click here to find a list of LIDODERM suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LIDODERM DMF (Drug Master File) is a document detailing the whole manufacturing process of LIDODERM active pharmaceutical ingredient (API) in detail. Different forms of LIDODERM DMFs exist exist since differing nations have different regulations, such as LIDODERM USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A LIDODERM DMF submitted to regulatory agencies in the US is known as a USDMF. LIDODERM USDMF includes data on LIDODERM's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The LIDODERM USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of LIDODERM suppliers with USDMF on PharmaCompass.
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