01 1Aurobindo Pharma Limited
02 3Bristol Myers Squibb
03 1Fermenta Biotech Limited
04 1GSK
05 1Sandoz B2B
06 1Blank
01 6DICLOXACILLIN SODIUM
02 1DICLOXACILLIN SODIUM MONOHYDRATE
03 1DICLOXACILLIN SODIUM USP
01 2India
02 1Switzerland
03 3U.S.A
04 1United Kingdom
05 1Blank
01 1Active
02 7Inactive
01 1Complete
02 7Blank
GDUFA
DMF Review : Complete
Rev. Date : 2020-05-26
Pay. Date : 2020-05-08
DMF Number : 19553
Submission : 2006-06-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13558
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13431
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13429
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13352
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13497
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13798
Submission : 1998-09-01
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13221
Submission : 1998-04-30
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
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PharmaCompass offers a list of Sodium Dicloxacillin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Sodium Dicloxacillin manufacturer or Sodium Dicloxacillin supplier for your needs.
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A Posipen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Posipen, including repackagers and relabelers. The FDA regulates Posipen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Posipen 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 Posipen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Posipen supplier is an individual or a company that provides Posipen active pharmaceutical ingredient (API) or Posipen finished formulations upon request. The Posipen suppliers may include Posipen API manufacturers, exporters, distributors and traders.
click here to find a list of Posipen suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Posipen DMF (Drug Master File) is a document detailing the whole manufacturing process of Posipen active pharmaceutical ingredient (API) in detail. Different forms of Posipen DMFs exist exist since differing nations have different regulations, such as Posipen USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Posipen DMF submitted to regulatory agencies in the US is known as a USDMF. Posipen USDMF includes data on Posipen's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Posipen USDMF is kept confidential to protect the manufacturer’s intellectual property.
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