Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1Nuray Chemicals Private Limited
02 1Chemische Fabrik Berg
03 13M Company
04 1Aurobindo Pharma Limited
05 1Cyalume Specialty Products
06 1Kreative Organics
07 1Micro Labs Limited
08 1Sai Life Sciences Limited
09 1Siegfried AG
10 2Blank
01 6METHENAMINE HIPPURATE
02 3METHENAMINE HIPPURATE USP
03 1METHENAMINE HIPPURATE USP (NON-STERILE DRUG SUBSTANCE)
04 1METHENAMINE HIPPURATE, USP
01 1Germany
02 5India
03 1Switzerland
04 2U.S.A
05 2Blank
01 7Active
02 4Inactive
01 5Complete
02 6Blank
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : Complete
Rev. Date : 2024-07-23
Pay. Date : 2024-07-08
DMF Number : 40057
Submission : 2024-07-04
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-10-27
Pay. Date : 2014-03-28
DMF Number : 28120
Submission : 2014-04-04
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7100
Submission : 1987-08-04
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-07-08
Pay. Date : 2013-04-15
DMF Number : 27021
Submission : 2013-04-09
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16801
Submission : 2003-08-08
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2021-11-24
Pay. Date : 2021-09-24
DMF Number : 34680
Submission : 2020-10-10
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-11-20
Pay. Date : 2017-10-16
DMF Number : 31988
Submission : 2017-10-06
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7333
Submission : 1988-02-08
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5018
Submission : 1983-07-29
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4949
Submission : 1983-05-23
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Methenamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methenamine, including repackagers and relabelers. The FDA regulates Methenamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methenamine 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 Methenamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methenamine supplier is an individual or a company that provides Methenamine active pharmaceutical ingredient (API) or Methenamine finished formulations upon request. The Methenamine suppliers may include Methenamine API manufacturers, exporters, distributors and traders.
click here to find a list of Methenamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Methenamine DMF (Drug Master File) is a document detailing the whole manufacturing process of Methenamine active pharmaceutical ingredient (API) in detail. Different forms of Methenamine DMFs exist exist since differing nations have different regulations, such as Methenamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Methenamine DMF submitted to regulatory agencies in the US is known as a USDMF. Methenamine USDMF includes data on Methenamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Methenamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Methenamine suppliers with USDMF on PharmaCompass.
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