Suanfarma, at the Core of a Better Life.
01 1Suanfarma
02 2Pfizer Inc
03 1Blank
01 4OXYTETRACYCLINE CALCIUM
01 1Spain
02 2U.S.A
03 1Blank
01 1Active
02 3Inactive
01 4Blank
Suanfarma, at the Core of a Better Life.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13389
Submission : 1998-09-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13369
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13453
Submission : 1998-09-01
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13670
Submission : 1998-09-01
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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A Bisolvomycin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bisolvomycin, including repackagers and relabelers. The FDA regulates Bisolvomycin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bisolvomycin 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 Bisolvomycin DMF (Drug Master File) is a document detailing the whole manufacturing process of Bisolvomycin active pharmaceutical ingredient (API) in detail. Different forms of Bisolvomycin DMFs exist exist since differing nations have different regulations, such as Bisolvomycin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
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