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 1Moehs Iberica
04 13M Company
05 1Aurobindo Pharma Limited
06 1Cyalume Specialty Products
07 1Kreative Organics
08 1Micro Labs Limited
09 1Recordati
10 1Sai Life Sciences Limited
11 1Siegfried AG
12 2Blank
01 1Germany
02 5India
03 1Italy
04 1Spain
05 1Switzerland
06 2U.S.A
07 2Blank
01 7Active
02 4Inactive
03 2Blank
01 13Blank
01 13Blank
01 1WC-0180
02 12Blank
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : Reviewed
Rev. Date : 2024-07-23
Pay. Date : 2024-07-08
DMF Number : 40057
Submission : 2024-07-04
Status : Active
Type : II
NDC Package Code : 58159-105
Start Marketing Date : 2024-10-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-10-27
Pay. Date : 2014-03-28
DMF Number : 28120
Submission : 2014-04-04
Status : Active
Type : II
NDC Package Code : 65319-1098
Start Marketing Date : 2019-06-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
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 : 16801
Submission : 2003-08-08
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-11-24
Pay. Date : 2021-09-24
DMF Number : 34680
Submission : 2020-10-10
Status : Active
Type : II
Date of Issue : 2022-08-29
Valid Till : 2025-07-26
Written Confirmation Number : WC-0180
Address of the Firm :
NDC Package Code : 58793-008
Start Marketing Date : 2016-12-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-07-08
Pay. Date : 2013-04-15
DMF Number : 27021
Submission : 2013-04-09
Status : Active
Type : II
NDC Package Code : 65862-808
Start Marketing Date : 2023-12-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7333
Submission : 1988-02-08
Status : Active
Type : II
NDC Package Code : 17381-305
Start Marketing Date : 2010-04-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29058
Submission : 2015-05-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7100
Submission : 1987-08-04
Status : Inactive
Type : II
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.
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