EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI
02 1TAPI Technology & API Services
03 1Celanese
04 1Curia
05 1F.I.S. Fabbrica Italiana Sintetici
06 1Ipca Laboratories
07 1Kalintis Healthcare
08 1Mangalam Drugs & Organics Ltd
09 1Olon S.p.A
10 1Plantex Ltd.
11 1SALSBURY CHEMICALS INC
12 1Sms Lifesciences
13 1Solmag
14 1Sri Krishna Pharmaceuticals
15 1Trifarma
16 6Blank
01 1ACTIVE & PLACEBO FUROSEMIDE (FRUSEMIDE TABS) 40MG
02 8FUROSEMIDE
03 1FUROSEMIDE (BULK)
04 11FUROSEMIDE USP
01 1France
02 5India
03 2Israel
04 4Italy
05 3U.S.A
06 6Blank
01 8Active
02 13Inactive
01 7Complete
02 14Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11785
Submission : 1995-12-18
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-11-20
Pay. Date : 2013-11-05
DMF Number : 2565
Submission : 1975-11-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1834
Submission : 1971-11-22
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-05-23
Pay. Date : 2016-02-23
DMF Number : 30288
Submission : 2016-02-29
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-03-16
Pay. Date : 2015-03-11
DMF Number : 3513
Submission : 1979-03-08
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-07-23
Pay. Date : 2013-07-15
DMF Number : 10109
Submission : 1993-02-23
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-08-29
Pay. Date : 2018-08-03
DMF Number : 33062
Submission : 2018-08-06
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2024-10-08
Pay. Date : 2024-09-24
DMF Number : 39960
Submission : 2024-07-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2649
Submission : 1976-04-02
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-07-11
Pay. Date : 2013-06-28
DMF Number : 23396
Submission : 2009-12-22
Status : Active
Type : II
A Diumide-K manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diumide-K, including repackagers and relabelers. The FDA regulates Diumide-K manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diumide-K 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 Diumide-K manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diumide-K supplier is an individual or a company that provides Diumide-K active pharmaceutical ingredient (API) or Diumide-K finished formulations upon request. The Diumide-K suppliers may include Diumide-K API manufacturers, exporters, distributors and traders.
click here to find a list of Diumide-K suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Diumide-K DMF (Drug Master File) is a document detailing the whole manufacturing process of Diumide-K active pharmaceutical ingredient (API) in detail. Different forms of Diumide-K DMFs exist exist since differing nations have different regulations, such as Diumide-K USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Diumide-K DMF submitted to regulatory agencies in the US is known as a USDMF. Diumide-K USDMF includes data on Diumide-K's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Diumide-K USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Diumide-K suppliers with USDMF on PharmaCompass.
We have 15 companies offering Diumide-K
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