TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.
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01 1Transo-Pharm USA LLC
02 1Biophore India Pharmaceuticals Pvt Ltd
03 2Nuray Chemicals Private Limited
04 1HRV Global Life Sciences
05 1TAPI Technology & API Services
06 1Azico Biophore India Pvt. Ltd
07 1Darmerica
08 1Fagron Group
09 1Fuan Pharmaceutical
10 1H. Lundbeck AS
11 1Letco Medical
12 2MSN Laboratories
13 2Medisca
14 1Pcca
15 2Blank
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01 1China
02 1Denmark
03 7India
04 1Israel
05 1Netherlands
06 5U.S.A
07 1United Kingdom
08 2Blank
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01 6Active
02 13Blank
01 2Valid
02 17Blank
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01 1218MF10985
02 18Blank
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01 1WC-0416
02 18Blank
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01 19Blank
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01 114501-0096
02 114501-0117
03 138779-0324
04 138779-3184
05 145562-1740
06 151552-1582
07 151927-0297
08 152952-003
09 158159-039
10 158159-124
11 162991-2857
12 169575-4025
13 171052-664
14 183511-003
15 183511-018
16 4Blank
01 19Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-01-19
Pay. Date : 2017-12-21
DMF Number : 32335
Submission : 2017-12-16
Status : Active
Type : II
Certificate Number : R0-CEP 2019-298 - Rev 02
Issue Date : 2023-05-15
Type : Chemical
Substance Number : 550
Status : Valid
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 : 2017-02-27
Pay. Date : 2016-12-26
DMF Number : 31249
Submission : 2017-01-27
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 : 58159-124
Start Marketing Date : 2025-04-25
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-039
Start Marketing Date : 2023-11-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-04-12
Pay. Date : 2018-08-17
DMF Number : 32771
Submission : 2018-05-07
Status : Active
Type : II
NDC Package Code : 52952-003
Start Marketing Date : 2012-07-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-06-02
Pay. Date : 2017-05-01
DMF Number : 7031
Submission : 1987-06-22
Status : Active
Type : II
Registration Number : 218MF10985
Registrant's Address : Via Quarta Strada, 2 Padova Italy
Initial Date of Registration : 2006-12-18
Latest Date of Registration :
NDC Package Code : 45562-1740
Start Marketing Date : 2001-02-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-01-26
Pay. Date : 2021-12-30
DMF Number : 35351
Submission : 2020-11-28
Status : Active
Type : II
Certificate Number : R0-CEP 2021-065 - Rev 00
Issue Date : 2023-03-03
Type : Chemical
Substance Number : 550
Status : Valid
NDC Package Code : 14501-0117
Start Marketing Date : 2025-03-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41534
Submission : 2025-03-28
Status : Active
Type : II
NDC Package Code : 14501-0096
Start Marketing Date : 2020-02-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Diazoxide 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 Diazoxide manufacturer or Diazoxide supplier for your needs.
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A NCGC00024907-08 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00024907-08, including repackagers and relabelers. The FDA regulates NCGC00024907-08 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00024907-08 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 NCGC00024907-08 supplier is an individual or a company that provides NCGC00024907-08 active pharmaceutical ingredient (API) or NCGC00024907-08 finished formulations upon request. The NCGC00024907-08 suppliers may include NCGC00024907-08 API manufacturers, exporters, distributors and traders.
click here to find a list of NCGC00024907-08 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 14 companies offering NCGC00024907-08
Get in contact with the supplier of your choice: