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 Pharma
05 1TAPI Technology & API Services
06 1Willow Birch Pharma
07 1Lundbeck CDM
08 1Azico Biophore India Pvt. Ltd
09 1Darmerica
10 1Fagron Group
11 1Fuan Pharmaceutical
12 1Letco Medical
13 2MSN Laboratories
14 2Medisca
15 1Pcca
16 1Yifan Pharmaceutical
17 3Blank
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01 2China
02 1Denmark
03 7India
04 1Israel
05 1Netherlands
06 6U.S.A
07 1United Kingdom
08 3Blank
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01 7Active
02 15Blank
01 2Valid
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01 1218MF10985
02 21Blank
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01 1WC-0021
02 1WC-0416
03 20Blank
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01 22Blank
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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 164181-0103
13 169575-4025
14 171052-664
15 183511-003
16 183511-018
17 6Blank
01 22Blank
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.
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
Lundbeck CDM delivers end-to-end API and drug product solutions from development to commercial scale.
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 : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
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 : 2026-12-31
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 : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 42890
Submission : 2025-10-30
Status : Active
Type : II

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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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PharmaCompass also assists you with knowing the Diazoxide API Price utilized in the formulation of products. Diazoxide API Price is not always fixed or binding as the Diazoxide Price is obtained through a variety of data sources. The Diazoxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diazoxide Choline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diazoxide Choline, including repackagers and relabelers. The FDA regulates Diazoxide Choline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diazoxide Choline 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 Diazoxide Choline supplier is an individual or a company that provides Diazoxide Choline active pharmaceutical ingredient (API) or Diazoxide Choline finished formulations upon request. The Diazoxide Choline suppliers may include Diazoxide Choline API manufacturers, exporters, distributors and traders.
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We have 16 companies offering Diazoxide Choline
Get in contact with the supplier of your choice: