Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1Amoli Organics
03 1Bayer AG
04 1Corden Pharma Bergamo S.p.A
05 1Erregierre SpA
06 1F.I.S. Fabbrica Italiana Sintetici
07 1Jiangsu Yuanyang Pharmaceutical
08 1SNJ Labs
09 1Shanghai Ziyuan Pharmaceutical
10 2Sifavitor srl
11 1Blank
01 7CLOTRIMAZOLE
02 1CLOTRIMAZOLE 250 MG ORAL TABLETS
03 2CLOTRIMAZOLE USP
04 1CLOTRIMAZOLE USP XX
05 1CLOTRIMAZOLE USP-EP
01 2China
02 1France
03 1Germany
04 2India
05 5Italy
06 1Blank
01 7Active
02 5Inactive
01 3Complete
02 9Blank
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 : 6729
Submission : 1986-12-17
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2020-09-17
Pay. Date : 2016-03-16
DMF Number : 26483
Submission : 2012-10-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6771
Submission : 1987-01-15
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-11-29
Pay. Date : 2016-11-14
DMF Number : 10713
Submission : 1994-02-04
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6324
Submission : 1986-03-01
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-01-07
Pay. Date : 2014-12-18
DMF Number : 7548
Submission : 1988-06-21
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9806
Submission : 1992-08-03
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5489
Submission : 1984-07-20
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35902
Submission : 2021-05-14
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5557
Submission : 1984-09-26
Status : Inactive
Type : II
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A Lotrimin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lotrimin, including repackagers and relabelers. The FDA regulates Lotrimin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lotrimin 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 Lotrimin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lotrimin supplier is an individual or a company that provides Lotrimin active pharmaceutical ingredient (API) or Lotrimin finished formulations upon request. The Lotrimin suppliers may include Lotrimin API manufacturers, exporters, distributors and traders.
click here to find a list of Lotrimin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lotrimin DMF (Drug Master File) is a document detailing the whole manufacturing process of Lotrimin active pharmaceutical ingredient (API) in detail. Different forms of Lotrimin DMFs exist exist since differing nations have different regulations, such as Lotrimin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lotrimin DMF submitted to regulatory agencies in the US is known as a USDMF. Lotrimin USDMF includes data on Lotrimin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lotrimin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lotrimin suppliers with USDMF on PharmaCompass.
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