Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
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01 1Nuray Chemicals Private Limited
02 1Biophore India Pharmaceuticals Pvt Ltd
03 1HRV Global Life Sciences
04 1Actavis Inc
05 1Apicore
06 1Apothecon Pharmaceuticals
07 2Azico Biophore India Pvt. Ltd
08 1BrightGene Bio-Medical Technology Co.,Ltd
09 1Curia
10 1Dasami Lab
11 1Emcure Pharmaceuticals
12 1Hetero Drugs
13 2MSN Laboratories
14 1ORGANICA Feinchemie GmbH Wolfen
15 1Optimus Pharma
16 1Piramal Pharma Solutions
17 1Prajna Generics
18 1SKVen Technologies Pvt. Ltd
19 1Sumitomo Chemical
20 1Suven Life Sciences Limited
21 1Suven Pharmaceuticals
22 1Viatris
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01 1China
02 1Germany
03 17India
04 1Ireland
05 1Japan
06 3U.S.A
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01 10Active
02 2Inactive
03 12Blank
01 24Blank
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01 1218MF10740
02 23Blank
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01 1WC-0042
02 1WC-0226
03 1WC-0281A3
04 1WC-0281new2
05 1WC-0369n
06 1WC-0404
07 1WC-0404A2
08 1WC-0416
09 16Blank
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01 24Blank
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01 114593-914
02 150379-0017
03 150379-0025
04 158159-031
05 159285-026
06 165392-2901
07 168022-7052
08 169575-4003
09 170966-0016
10 176339-133
11 14Blank
01 24Blank
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 : 2016-12-23
Pay. Date : 2016-09-13
DMF Number : 30878
Submission : 2016-11-08
Status : Active
Type : II
Date of Issue : 2024-02-20
Valid Till : 2026-12-06
Written Confirmation Number : WC-0416
Address of the Firm :
NDC Package Code : 58159-031
Start Marketing Date : 2024-12-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-03-01
Pay. Date : 2015-09-15
DMF Number : 29527
Submission : 2015-09-03
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-09-14
Pay. Date : 2017-08-17
DMF Number : 31085
Submission : 2016-12-02
Status : Active
Type : II
Date of Issue : 2020-04-15
Valid Till : 2023-05-19
Written Confirmation Number : WC-0281new2
Address of the Firm :
NDC Package Code : 50379-0025
Start Marketing Date : 2023-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-09-03
Pay. Date : 2018-07-17
DMF Number : 32956
Submission : 2018-07-19
Status : Active
Type : II
Date of Issue : 2019-07-15
Valid Till : 2022-07-14
Written Confirmation Number : WC-0042
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37777
Submission : 2022-12-16
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-10-23
Pay. Date : 2020-06-19
DMF Number : 34910
Submission : 2020-08-28
Status : Active
Type : II
NDC Package Code : 70966-0016
Start Marketing Date : 1985-11-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-04-17
Pay. Date : 2017-02-22
DMF Number : 31395
Submission : 2017-02-23
Status : Active
Type : II
Date of Issue : 2019-10-07
Valid Till : 2022-07-02
Written Confirmation Number : WC-0226
Address of the Firm :
NDC Package Code : 14593-914
Start Marketing Date : 2023-09-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32113
Submission : 2017-12-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5351
Submission : 1984-05-17
Status : Inactive
Type : II
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PharmaCompass offers a list of Trientine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Trientine Hydrochloride manufacturer or Trientine Hydrochloride supplier for your needs.
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A Trientine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trientine Dihydrochloride, including repackagers and relabelers. The FDA regulates Trientine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trientine Dihydrochloride 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 Trientine Dihydrochloride supplier is an individual or a company that provides Trientine Dihydrochloride active pharmaceutical ingredient (API) or Trientine Dihydrochloride finished formulations upon request. The Trientine Dihydrochloride suppliers may include Trientine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Trientine Dihydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 22 companies offering Trientine Dihydrochloride
Get in contact with the supplier of your choice: